Tag: M.W=100-150

Yang, Yong published the artcileComplete chloroplast genome sequence of the mangrove species Kandelia obovata and comparative analyses with related species., Recommanded Product: Phthalonitrile, the main research area is Chloroplast genome; Kandelia obovata; Mangrove species; Phylogeny comparative analysis.

As one of the most cold and salt-tolerant mangrove species, Kandelia obovata is widely distributed in China. Here, we report the complete chloroplast genome sequence K. obovata (Rhizophoraceae) obtained via next-generation sequencing, compare the general features of the sampled plastomes of this species to those of other sequenced mangrove species, and perform a phylogenetic analysis based on the protein-coding genes of these plastomes. The complete chloroplast genome of K. obovata is 160,325 bp in size and has a 35.22% GC content. The genome has a typical circular quadripartite structure, with a pair of inverted repeat (IR) regions 26,670 bp in length separating a large single-copy (LSC) region (91,156 bp) and a small single-cope (SSC) region (15,829 bp). The chloroplast genome of K. obovata contains 128 unique genes, including 80 protein-coding genes, 38 tRNA genes, 8 rRNA genes and 2 pseudogenes (ycf1 in the IRA region and rpl22 in the IRB region). In addition, a simple sequence repeat (SSR) analysis found 108 SSR loci in the chloroplast genome of K. obovata, most of which are A/T rich. IR expansion and contraction regions were compared between K. obovata and five related species: two from Malpighiales and three mangrove species from different orders. The mVISTA results indicated that the genome structure, gene order and gene content are highly conserved among the analyzed species. The phylogenetic analysis using 54 common protein-coding genes from the chloroplast genome showed that the plant most closely related to K. obovata is Ceriops tagal of Rhizophoraceae. The results of this study provide useful molecular information about the evolution and molecular biology of these mangrove trees.

PeerJ published new progress about Chloroplast genome; Kandelia obovata; Mangrove species; Phylogeny comparative analysis. 91-15-6 belongs to class nitriles-buliding-blocks, name is Phthalonitrile, and the molecular formula is C8H4N2, Recommanded Product: Phthalonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Hatano, Kouta published the artcileSyntheses of 2,4-dicyanophenoxyacetic acid and its analogs, Category: nitriles-buliding-blocks, the main research area is cyanophenoxyacetate pesticide; phenoxyacetate cyano pesticide.

Cyanophenoxyacetic acids (I; R = H; R1 = H, CN; R2 = Me, H, CN) and their Et esters (I; R = Et) were prepared in order to test their pesticidal properties. E.g. Reimer-Tiemann reaction of o-HOC6H4CHO, followed by refluxing the resulting 2,4-(OHC)2C6H3OH with NH2OH.HCl in AcOH gave 2,4-(NC)2C6H3OH which reacted with BrCH2CO2Et to give I (R = Et, R1 = R2 = CN). The other I were prepared similarly.

Agricultural and Biological Chemistry published new progress about cyanophenoxyacetate pesticide; phenoxyacetate cyano pesticide. 34133-58-9 belongs to class nitriles-buliding-blocks, name is 4-Hydroxyisophthalonitrile, and the molecular formula is C8H4N2O, Category: nitriles-buliding-blocks.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Khajeh Dangolani, Soheila published the artcileImmobilized palladium nanoparticles on a cyclodextrin-polyurethane nanosponge (Pd-CD-PU-NS): An efficient catalyst for cyanation reaction in aqueous media, Recommanded Product: 2-Aminobenzonitrile(Flakes or Chunks), the main research area is palladium nanoparticle cyclodextrin polyurethane nanosponge catalyst cyanation reaction.

Immobilized palladium nanoparticles on a cyclodextrin-polyurethane nanosponge (Pd-CD-PU-NS) were found to be an efficient heterogeneous catalyst in the cyanation reaction of aryl halides in aqueous media. This catalyst system is containing palladium nanoparticles with a size of � nm. Moreover, the CD-PU-NS support formed microsphere-shaped structures with a size of �00-200 nm. The TEM images show that Pd nanoparticles were formed in near spherical shape morphol. and were immobilized in the structure of the CD-PU-NS support. Under our optimized reaction conditions, aryl cyanides were obtained in high yields in the presence of the Pd-CD-PU-NS catalyst. Our results demonstrated that the Pd-CD-PU-NS catalyst is highly effective in the cyanation reaction in aqueous media. Furthermore, the catalyst could be simply extracted from the reaction mixture, providing an efficient methodol. for the synthesis of aryl cyanides. The Pd-CD-PU-NS catalyst could be recycled four times with almost consistent catalytic efficiency.

Inorganica Chimica Acta published new progress about Cyanation. 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Recommanded Product: 2-Aminobenzonitrile(Flakes or Chunks).

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Cai, Mingzhong published the artcileRecyclable and Reusable Pd(OAc)2/XPhos-SO3Na/PEG-400/H2O System for Cyanation of Aryl Chlorides with Potassium Ferrocyanide, SDS of cas: 100-70-9, the main research area is reusable palladium acetate XPhos sulfonate catalyst cyanation aryl chloride.

Pd(OAc)2/XPhos-SO3Na in a mixture of poly(ethylene glycol) (PEG-400) and water is shown to be a highly efficient catalyst for the cyanation of aryl chlorides with potassium ferrocyanide. The reaction proceeded smoothly at 100 or 120°C with K2CO3 or KOAc as base, delivering a variety of aromatic nitriles in good to excellent yields. The isolation of the crude products is facilely performed by extraction with cyclohexane and more importantly, both expensive Pd(OAc)2 and XPhos-SO3Na in PEG-400/H2O system could be easily recycled and reused at least six times without any apparent loss of catalytic efficiency.

Catalysis Letters published new progress about Cyanation. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, SDS of cas: 100-70-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Xu, Feng published the artcileHypervalent Iodine(III)-Mediated Regioselective Cyanation of Quinoline N-Oxides with Trimethylsilyl Cyanide, Recommanded Product: Picolinonitrile, the main research area is hypervalent iodine regioselective cyanation quinoline oxide trimethylsilyl cyanide; cyanoquinoline preparation.

A regioselective cyanation of quinoline N-oxides with trimethylsilyl cyanide was developed by using (Diacetoxyiodo) benzene (PIDA) as mediated hypervalent iodine(III) reagent under metal-free and base-free reaction conditions to obtain 2-cyanoquinolines. The efficient PIDA reagent could play the role of an activator of the substrates and an accelerator of N-O bond cleavage. The reaction system featured a wide range of substrate suitability and high yields. The procedure was enlarged gram-scale to synthesize the tuberculosis (TB) inhibitor. Finally, according to some exptl. results, a plausible mechanism for the cyanation reaction is proposed.

Advanced Synthesis & Catalysis published new progress about Cyanation. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Recommanded Product: Picolinonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Begum, Robina published the artcileReduction of nitroarenes catalyzed by microgel-stabilized silver nanoparticles, Related Products of nitriles-buliding-blocks, the main research area is nitroarene reduction microgel stabilized silver nanoparticle; Ag nanoparticles; Aryl amines; Catalytic reduction; Nitroarenes.

Poly(N-isopropylacrylamide-co-acrylamide) (PNA-BIS-2) microgels were synthesized by free radical precipitation polymerization in aqueous medium. Spherical Ag nanoparticles with diameter of 10-20 nm were fabricated inside the PNA-BIS-2 microgels by in-situ reduction of silver nitrate using sodium borohydride as reducing agent. The Ag nanoparticles- loaded hybrid microgels were characterized by SEM (SEM), Transmission electron microscopy (TEM), Energy dispersive X-ray (EDX), Scanning transmission electron microscopy (STEM), UV visible spectroscopy (UV Visible), Thermogravimetric anal. (TGA) and X-ray diffraction (XRD). Ag contents in the hybrid system were determined by inductively coupled plasma – optical emission spectrometry (ICP-OES). Various nitroarenes were successfully converted into their resp. aromatic amines with good to excellent yields (ranging from 75% to 97%) under mild reaction conditions. The catalyst has ability to successfully convert substituted nitroarenes into desired products keeping many functionalities intact. The catalyst can be stored for long time without any sign of aggregation and can be used multiple times without any significant loss in its catalytic activity.

Journal of Hazardous Materials published new progress about Microgels. 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Related Products of nitriles-buliding-blocks.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Dorman, P. Matisha published the artcileAn analysis of the rotational ground state and lowest-energy vibrationally excited dyad of 3-cyanopyridine: Low symmetry reveals rich complexity of perturbations, couplings, and interstate transitions, Recommanded Product: Picolinonitrile, the main research area is cyanopyridine perturbation coupling interstate transition rotational ground state.

The rotational spectrum of 3-cyanopyridine from 130 to 360 GHz was recorded, and an anal. of the ground state and two lowest-energy excited vibrational states was completed. Almost 6700 new transitions were measured for the ground state and fit to a partial octic, distorted-rotor Hamiltonian with low error (σfit < 0.05 MHz). The first two excited vibrational states, ν30 and ν21, are an isolated dyad that exhibits both a- and b-type Coriolis perturbations and requires a two-state, least-squares fit to fully predict the rotational spectrum and determine accurate spectroscopic constants Quartic and sextic distortion constants were determined for the dyad, along with seven symmetry-allowed perturbation terms: Ga, GaJ, Fbc, FbcK, Gb, GbJ, and GbK. Numerous resonances, including those following a-type selection rules, ΔKa = 2 or ΔKa = 4, and b-type selection rules, ΔKa = 3 or ΔKa = 5, were observed and fit. For ν30 and ν21, the energy difference (ΔE30,21 = 15.7524693 (37) cm-1), both Coriolis coupling constants (ζ30,21a = 0.8327 (9) and ΔE30,21b = -0.0181 (3)), and vibration-rotation interaction constants were determined exptl. and compared to theor. values determined computationally. Combined with the work on the vibrationally excited dyads of 4-cyanopyridine, Ph isocyanide, benzonitrile, and phenylacetylene, the coupling in ν30 and ν21 provides an opportunity to compare the Coriolis interactions of these analogus mono-substituted aromatic mols. in unusual detail. Addnl., this work improves the ground-state rotational constants and centrifugal distortion constants of 3-cyanopyridine and provides the fundamental constants needed to support an astronomical search for 3-cyanopyridine in the interstellar medium. Journal of Molecular Spectroscopy published new progress about Analysis. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Recommanded Product: Picolinonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Cai, Xue published the artcileDimeric phthalocyanine-involved double-decker complex-based electrochemical sensor for simultaneous detection of acetaminophen and ascorbic acid, Application of Phthalonitrile, the main research area is acetaminophen ascorbic acid phthalocyanine double decker complex electrochem sensor.

An electrochem.sensor for simultaneous detection of acetaminophen (APAP) and ascorbic acid (AA) is firstly developed by using the self-assembled film of a novel dimeric bis(phthalocyaninato) europium complex, [{Pc(SC2H5)8}Eu{BiPc(SC2H5)12}Eu{Pc(SC2H5)8}] (1) coated onto ITO (fim-1/ITO) fabricated through a solution-processing quasi-LangmuirShafer (QLS) protocol. A combination of unique sandwich mol.structure with extented π-conjugated system and J-type aggregates with quite uniform nanograins (ca.15 nm) formed on ITO substrate render the film of 1 the excellent charge transfer ability and abundant electroactive sites, resulting in sensitive detection of APAP and AA with the good sensitivities of 254 and 85.6 mA μM-1 cm-2 and low detection limits of 1.3 and 3.7 μM for APAP and AA resp. More importantly, a simultaneous determinationof APAP and AA at a coexisting system of APAP and AA is also achieved with the still good sensitivities of 317 and 64.7 mA μM-1 cm-2, and low detection limits of 1.0 and 4.9 μM for APAP and AA resp. This work represents the first example of tetrapyrrole-based organicsemiconductor electrochem.sensor for simultaneous detection of APAP and AA with excellent sensing performance, implying the great application potential of electroactive sandwich rare earth tetrapyrrole compoundsin the nonenzymic electrochem.sensors.

Journal of Materials Science: Materials in Electronics published new progress about Analysis. 91-15-6 belongs to class nitriles-buliding-blocks, name is Phthalonitrile, and the molecular formula is C8H4N2, Application of Phthalonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Zhao, Yun-Xiu published the artcileNeonicotinoid thiacloprid transformation by the N2-fixing bacterium Microvirga flocculans CGMCC 1.16731 and toxicity of the amide metabolite, Recommanded Product: Picolinonitrile, the main research area is Microvirga Daphnia neonicotinoid thiacloprid transformation amide metabolite toxicity.

Thiacloprid is a widely-used neonicotinoid insecticide, but its enzymic conversion and the toxicity of the amide metabolite are poorly understood. Here, a N2-fixing bacterium, Microvirga flocculans CGMCC 1.16731, was reported to metabolize thiacloprid via hydration and hydroxylation to thiacloprid amide and 4-hydroxy thiacloprid resp. M. flocculans transformed 90.5% of 0.63 mmol/L thiacloprid in 30 h with a half-life of 9.0 h. In soil, the bacterium transformed 92.4% of 80 μmol/kg soil thiacloprid in 9 d. A cobalt-type nitrile hydratase (NHase) composed of an α-subunit (TnhA) and a β-subunit (TnhB) converted thiacloprid to thiacloprid amide. Co-expression of activator (TnhC) with NHase could improve the TnhA solubility and therefore enhanced 4-folds higher NHase activity. The NHase produced recombinantly in Escherichia coli transformed 97% of 0.76 mmol/L thiacloprid in 10 min. M. flocculans NHase had a Km value of 0.63 mmol/L and Vmax of 10.2 μmol/min/mg toward thiacloprid. Thiacloprid amide has higher toxic effect on growth of M. flocculans than thiacloprid, whereas lower toxic on the aquatic invertebrate Daphnia magna. Both thiacloprid and thiacloprid amide inhibited tnhA transcription. This increases our understanding of the enzymic mechanism of environmental fate of thiacloprid and toxicity of its amide metabolite toward soil microbes and aquatic organisms.

International Biodeterioration & Biodegradation published new progress about Aquation. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Recommanded Product: Picolinonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Manning, Trevor W. published the artcileStructure of an unusual tetracyclic deoxyguanosine adduct: Implications for frameshift mutagenicity of ortho-cyano nitroanilines, Recommanded Product: 2-Aminobenzonitrile(Flakes or Chunks), the main research area is structure tetracyclic deoxyguanosine adduct frameshift mutagenicity orthocyanonitroaniline.

Nitroarom. compounds represent a major class of industrial chems. that are also found in nature. Polycyclic derivatives are regarded as potent mutagens and carcinogens following bioactivation to produce nitrenium electrophiles that covalently modify DNA to afford N-linked C8-2′-deoxyguanosine (C8-dG) lesions that can induce frameshift mutations, especially in CpG repeat sequences. In contrast, their monocyclic counterparts typically exhibit weak mutagenicity or a lack thereof, despite also undergoing bioactivation to afford N-linked C8-dG adducts. Recently, it has been reported that cyano substitution can greatly increase the mutagenicity of nitroaniline derivatives that are components of azo dyes. The basis of this “”cyano effect”” may be rooted in the formation of a novel polycyclic adduct arising from initial formation of the N-linked C8-dG adduct followed by a cyclization process involving N7 of dG and the ortho-CN group of the attached C8-aryl moiety to generate a quinazolinimine ring as part of a fused tetracyclic C8,N7-dG adduct structure. The present work structurally characterizes this novel cyclic adduct using a combination of optical spectroscopies, NMR anal., d. functional theory (DFT) calculations, and mol. dynamics (MD) simulations. Our data indicate that this highly fluorescent cyclic adduct adopts the promutagenic syn conformation and can stabilize the slipped mutagenic intermediate (SMI) within the CpG repeat of the NarI sequence, which is a hotspot for frameshift mutagenesis mediated by polycyclic N-linked C8-dG adducts. In contrast, the open para-CN (4-aminobenzontrile-derived) N-linked C8-dG adduct is less likely to disrupt the canonical B-form. Together, our results provide a rationale for the potent mutagenicity of cyano-substituted nitroaniline derivatives recently reported in frameshift-sensitive tester strains.

Chemical Research in Toxicology published new progress about Azo dyes. 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Recommanded Product: 2-Aminobenzonitrile(Flakes or Chunks).

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts