Ciano-, Nitrilo-

4-Hydroxyphenylacetonitrile (HPA) is a chemical compound that belongs to the group of nitriles. It is a precursor to the pigment sinalbin, which is found in corynebacterium and related bacteria. HPA has been shown to have an apoptotic effect on human cells, which may be due to its ability to inhibit protein synthesis and induce DNA fragmentation. The synthetic pathway for HPA starts with the conversion of L-phenylalanine into 4-hydroxyphenylpyruvic acid by a wild-type strain or bacterial strain. The 4-hydroxyphenylpyruvic acid is then converted into 4-hydroxybenzaldehyde through polymerase chain reactions or expression plasmids in corynebacterium glutamicum. This molecule can then be transformed into HPA by hydrolysis with hydrochloric acid or enzymatic activity. HPA has also been shown to stimulate

Azobis(4-cyanovaleric acid) is a chemical compound that has reactive functional groups. It is a particle that is soluble in acetate extract and hydrochloric acid. The synthesis of Azobis(4-cyanovaleric acid) involves the reaction of 4-cyanoacrylic acid with 2,2'-azobis(2-methylpropionitrile). It is used as an intermediate in the preparation of polymers. Azobis(4-cyanovaleric acid) is used for the treatment of infectious diseases such as tuberculosis and malaria. The production of chain reactions with other molecules makes this chemical reactive and unstable. Azobis(4-cyanovaleric acid) also reacts with nucleophilic groups, such as hydroxyl groups, to form a covalent bond. This process can be reversed by adding a strong base or oxidant.

2-Chloro-4-fluorobenzonitrile is a drug that has been shown to have antitumor effects by binding to the CB2 receptor. It inhibits hydrogenation reduction of the molecule, which may be due to its ability to react with both functional groups. 2-Chloro-4-fluorobenzonitrile has also been shown to inhibit progesterone receptor, which may lead to an increase in progesterone levels and a decrease in estrogen levels. The pharmacokinetic properties of this compound are not yet known.

Cyanomethyl)urea is a fine chemical that belongs to a class of compounds known as ureas. It is used as a versatile building block in the synthesis of more complex compounds, as a research chemical and as an intermediate. It can be used to synthesize pharmaceuticals, pesticides, and other chemicals. Cyanomethyl)urea is used in the production of polyurethane foams, which are commonly found in mattresses, furniture upholstery and insulation.

Cyanodibenzylamine is a synthetic, pharmaceutical preparation. It is an amine that undergoes nucleophilic attack by an amide to form a cyanoguanidine. Cyanodibenzylamine can be used as a stabilizer and additive in pharmaceutical preparations. It also has the ability to bind metal hydroxides, which may be due to the presence of basic fibroblast growth factor and isoquinoline compound. Cyanodibenzylamine is also used as a polymerization initiator in organic chemistry, with hydrocarbon solvents such as benzene or toluene as its solvent.

2-Acetoxybenzonitrile is an atypical, acidic organic compound with a molecular weight of 136.06 g/mol. It has a melting point of -5.5 °C and decomposes spontaneously at high temperatures to form benzonitrile, carbon dioxide, and water. 2-Acetoxybenzonitrile is able to act as a competitive inhibitor of acetylsalicylic acid (ASA) in the kinetic determination of ASA using acetylation as the rate-determining step. In this experiment, 2-acetoxybenzonitrile was found to be an effective inhibitor of acetylation with a KI value of 1.8 x 10 M. The spectrometer can be used to determine the molecular weight and purity of 2-acetoxybenzonitrile by measuring its absorbance in the ultraviolet region.
2-Acetoxybenzonitrile binds metal cations such as Cu(II), Fe(

4-Cyanocinnamic acid is a fatty acid that has been shown to be a substrate for the bacterial enzyme cinnamate 4-hydroxylase. The molecular weight of this compound is 136.16 g/mol, and it has a constant boiling point of 206°C. It can be synthesized from phenylacetic acid and p-coumaric acid using a transesterification reaction. This compound is reactive with carbonyl groups, which makes it useful in the detection of gram-positive bacteria by fluorescent probes or fluorescent dyes. 4-Cyanocinnamic acid is unreactive with esters of carboxylic acids, such as methyl esters, making it useful for the determination of fatty acids in isolates.

3-Cyano-5-bromopyridine is an enantiopure organic compound that belongs to the group of halides. It is a functional group that is a reagent in organic synthesis, and it can be used as a precursor to dyestuffs. 3-Cyano-5-bromopyridine has been shown to have antimicrobial activity against bacteria and fungi. It also has a metabotropic glutamate receptor subtype selective affinity, which may be due to its ability to bind with glutamate in complex molecules.

2-Cyanocinnamic acid is a fatty acid that has been shown to inhibit the synthesis of proteins. It binds to cytochrome c oxidase, inhibiting mitochondrial respiration and electron transport, leading to decreased ATP production. 2-Cyanocinnamic acid is not easily transported out of mitochondria, which leads to its accumulation in the mitochondrial matrix. This accumulation causes synergistic inhibition with glutamate, leading to a decrease in ATP production and an increase in intracellular levels of reactive oxygen species (ROS). The use of 2-cyanoacrylic acid as a mitochondrial transport inhibitor has been proposed for the treatment of obesity and diabetes.
2-Cyanocinnamic acid also inhibits fatty acid uptake by binding to the protein translocase at the outer membrane of cells. This binding prevents monomers from entering the cell, where they are broken down by beta oxidation and converted into acetyl-CoA, which can be used for energy production or stored as triglycer

3,4-Difluoro-5-nitrobenzonitrile is a hepatotoxic compound that is found in the environment. It has been shown to cause cirrhosis and overgrowth of the liver. 3,4-Difluoro-5-nitrobenzonitrile also inhibits hepatic encephalopathy and may be used to treat liver disease. This toxicant has been detected in the bowel and duodenum of humans with nonalcoholic steatohepatitis, as well as in the jejunum and duodenum of mice with spontaneous steatohepatitis. It also causes nonalcoholic steatohepatitis when given orally to rats.

4-Cyano-2-hydroxybenzaldehyde is a high quality chemical that can be used as a reagent and intermediate in the synthesis of complex compounds. It is also an important building block in the synthesis of fine chemicals. 4-Cyano-2-hydroxybenzaldehyde has been used as a versatile building block in the synthesis of organic compounds, useful scaffolds in medicinal chemistry, and reactive intermediates. It has also been shown to have anti-inflammatory properties and may be a potential treatment for inflammatory bowel disease.

N-Nitrosodibenzylamine is a chemical compound that has genotoxic effects. It is used as an analytical method to identify the presence of amines and to measure their concentration, as well as in the preparation of sodium salts. N-Nitrosodibenzylamine was found to cause damage to DNA in animals and cells in culture. The matrix effect, which is the difference in response between a sample contained in an organic solvent and one contained in water, was investigated using multi-walled carbon nanotubes (MWCNTs). The results showed that MWCNTs produce a significant matrix effect when compared with other solvents. This study also showed that MWNTs have a higher capacity for nitrosamine adsorption than do other solvents.

Xylene cyanol is a chemical compound that belongs to the group of phenols. It has been shown to be active in vitro against human skin cancer cells, and induces cell lysis. Xylene cyanol has also been found to bind to the BCR-ABL kinase domain, which is an enzyme that plays a crucial role in the development of leukemia and other autoimmune diseases. Xylene cyanol binds to dna binding domains on the protein surface and forms an adduct with bcr-abl kinase, which inhibits its activity. This inhibition prevents activation of this enzyme and leads to cell death by preventing DNA synthesis.

(2,3-Dichlorophenyl)acetonitrile is a fine chemical that is useful as a building block in the synthesis of more complex compounds. It has been used in research as a reagent and as a speciality chemical. (2,3-Dichlorophenyl)acetonitrile reacts with many different types of compounds to form new molecules. This intermediate can be used in the synthesis of many different types of compounds and also serves as an important scaffold for larger molecules.

4-Amino-2-cyanotoluene is a quinazoline compound that inhibits the synthesis of thymine, which is necessary for DNA replication. This compound binds to the enzyme thymidylate synthetase, thereby inhibiting the synthesis of thymine. The inhibitory effect has been shown in a study using calf thymus DNA. 4-Amino-2-cyanotoluene also inhibits the synthesis of other nucleic acids such as adenine and guanine.

4-Aminophenylacetonitrile is a molecule that is structurally similar to nitrobenzene. 4-Aminophenylacetonitrile has been shown to be an efficient method for inhibiting faecalis growth and secretory phospholipase A2 (sPLA2) activity in vitro. It also inhibits the population growth of E. coli in vivo, which can be attributed to its ability to inhibit the enzyme catalysed by hydrogen bond formation.

4-Cyanobenzylamine HCl is a degradable polymer that has been shown to inhibit colonic adenocarcinoma in mice. This compound was synthesized by the reaction of 4-cyanobenzylamine with 3-mercaptopropionic acid and was characterized using IR, 1H NMR, and 13C NMR spectroscopy. It also showed an inhibitory effect on the proliferation of human colon cancer cells. The polymer was found to gel when mixed with different concentrations of acrylamide and methylene bisacrylamide. Gelation occurred at a lower concentration of acrylamide than the amount used in previous studies. This may be due to its functional groups and morphology, which could have contributed to the inhibition of cell growth.

1-Adamantyl acetonitrile is a trifluoroacetic acid derivative that is used in the synthesis of 4-aminoantipyrine, chlorides, acid chlorides, and acetonitrile. 1-Adamantyl acetonitrile can be used to produce a variety of pharmaceuticals, such as aliphatic carboxylic acids, aldehydes, and amide. It can also serve as a reactant for reactions with alcohols or amines.

2-Cyanoacetamide is an organic compound that is used in pharmaceutical preparations. It reacts with malonic acid to form a dioxime, which is a precursor of various drugs. The optimum concentration for the reaction to occur is at 10% (w/v). The reaction mechanism has not been fully elucidated and it involves the transfer of nitrogen from an amide group to a carbonyl group. 2-Cyanoacetamide has shown anti-angiogenic effects in mice by inhibiting the expression of Mcl-1 protein, which is involved in the regulation of apoptosis and inflammation. This drug also has biological functions as a precursor for dopamine, which helps regulate motor and cognitive functions.

2-Cyano-3-fluoro-4-bromo aniline is a plant growth regulator that can be used to prevent and control the spread of viral diseases in plants. 2-Cyano-3-fluoro-4-bromo aniline inhibits the replication of influenza virus strains by binding to the viral coat protein. It also has been shown to inhibit proteolytic enzymes when applied as a coating on particles. The main mechanism of this compound is through its ability to bind to regulatory proteins, which prevents them from binding with other regulatory proteins and activating transcription factors. The expression profile suggests that this compound may regulate the expression of genes involved in plant development, cell division, and response to stress.

4-Cyanobenzamide is a naphthalene derivative that is both reactive and intramolecular. It has been shown to react with the amino group of peptides, forming a ruthenium complex. The functional groups are acceptors and donors that can be used in assays for the detection of anions or cations. 4-Cyanobenzamide reacts with water to release hydrogen gas, which can be used to measure its hydration ability. This compound has been synthesized using solid-phase synthesis and it has amide bonds that vibrate at a specific frequency.

2-Bromo-5-chlorophenylacetonitrile is an organic compound that is used as a reagent and building block in the synthesis of other chemicals. It is a colourless liquid that can be used to synthesize complex compounds. 2-Bromo-5-chlorophenylacetonitrile has been shown to be useful in the synthesis of pharmaceuticals, pesticides, and herbicides. This chemical can be used as a versatile intermediate or building block for the production of high quality research chemicals and specialty chemicals. 2-Bromo-5-chlorophenylacetonitrile is not on the list of chemical substances classified as hazardous according to EU regulation (EINECS) No. 231-1003.

Substrate of benzylamine oxidase and monoamine oxidase B

N-Cyanopyrrolidine is a compound that targets enzymes, such as histone deacetylases (HDACs) and protein kinase C. It is a chemical ionization reagent that reacts with hydroxyl groups on the target molecule. This leads to the formation of covalent bonds between the target and the reagent, which results in an irreversible reaction. N-Cyanopyrrolidine has been shown to have antidiabetic effects in diabetic patients and hiv infection by decreasing levels of glucose in the blood. It also inhibits cancer cell growth by inhibiting dpp-IV, which is an enzyme that causes cancer cells to proliferate.

2-Chloro-5-methylbenzonitrile (2C5MB) is a versatile building block that is used in the production of fine chemicals, specialty chemicals, and pharmaceuticals. It is also used as a reagent for organic synthesis and as a speciality chemical. 2C5MB can be used in the synthesis of various complex compounds and research chemicals. The compound has been shown to have high reactivity and has been used as a reaction component or scaffold for the synthesis of other products.

2-Cyanobenzylamine hydrochloride is a chemical building block and intermediate that can be used in the synthesis of many different compounds. It is also a useful reagent for reactions involving nitro compounds. 2-Cyanobenzylamine hydrochloride is a fine chemical that is registered with the Chemical Abstract Service (CAS No. 1134529-25-1). It has been identified as a versatile building block and useful intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic chemicals.

3-Cyano-2-hydroxypyridine is an inhibitor of the noradrenaline transporter, which is a type of l-type calcium channel. 3-Cyano-2-hydroxypyridine has been shown to be a potent inhibitor of the noradrenaline transporter. It inhibits the binding of neurotransmitters to their receptors by blocking active methylene sites on the transporter molecule. This drug also has a cavity that can accommodate bulky inhibitor molecules, making it more difficult for these inhibitors to bind to the active site and compete with neurotransmitters for uptake. 3Cyano-2-hydroxypyridine also inhibits nitric oxide synthase, which may provide anti-tumor activity as well as inhibit tumor cell growth. The inhibitory effect of this drug is due to structural studies that have revealed hydrogen bonding interactions with the drug's nitrogen and oxygen atoms.

2-Nitrobenzylamine hydrochloride is a compound that has been shown to have cancer-fighting properties. It inhibits the synthesis of proteins necessary for the proliferation of cancer cells, but it does not affect the synthesis of proteins in healthy cells. This drug is used to diagnose and treat certain types of cancers, such as lymphoma and leukemia. 2-Nitrobenzylamine hydrochloride can be modified by genetic engineering techniques to specifically target cancer cells, which may help with the treatment of other types of diseases in the future. It is believed that this drug will be useful for treating cancers that are resistant to chemotherapy or radiation therapy, as well as those that are caused by mutations in DNA.

Cyano ethyl acetamidate is a synthetic compound that is used in the production of immunosorbent assays. It is a reaction yield and amide. This product has been shown to be an effective amination reagent in deionized water and wastewater, as well as a powerful monoclonal antibody producer. Cyano ethyl acetamidate has also been shown to be reactive with chloride and hydrogen chloride, which can be used for the synthesis of nitro compounds.

3-Bromobenzylamine is a chemical compound that belongs to the class of amines. It is used as an intermediate in organic synthesis, and its derivative 3-bromobenzylamine hydrochloride is used in pharmaceuticals as a heart stimulant. 3-Bromobenzylamine can be synthesized by reacting an amine with phosgene and then brominating it. This chemical has been shown to have inhibitory activity against cancer cells and can be used for the treatment of cancer. 3-Bromobenzylamine has also been shown to inhibit the growth of bacteria, fungi, and viruses in vitro. 3-Bromobenzylamine may also be useful for treating psoriasis due to its ability to inhibit prostaglandin synthesis.

2-Cyanoethyltriethoxysilane is a cross-linking agent that is used in coatings and adhesives. It has been shown to have an adsorption mechanism that is dependent on the pH of the solution, with a maximum adsorption at pH 3.2 and a minimum at pH 11. The rate of adsorption is also dependent on the concentration of 2-cyanoethyltriethoxysilane, with higher concentrations leading to faster adsorption rates. Kinetic data for 2-cyanoethyltriethoxysilane has been shown using gravimetric analysis to show that it has an adsorption rate constant of 1.0 × 10^4 s^(-1) at pH 3.2 and 6.5 × 10^4 s^(-1) at pH 11, which are independent of the concentration of this molecule in solution. Pluronic P123 was used as a model polymer

2-[1,2,4]Triazol-1-yl-benzylamine is a chemical compound that has been shown to be an excellent reagent in organic synthesis. It is also used as a building block for the synthesis of compounds related to pharmaceuticals, pesticides and other speciality chemicals. 2-[1,2,4]Triazol-1-yl-benzylamine is a versatile intermediate that can be used in the synthesis of complex compounds with good yields and high purity.

2-(4-Methoxyphenoxy)acetonitrile is a chemical compound that is used to synthesize acetobromoglucose. It undergoes transformation and condensation reactions with acetobromoglucose to form 4-methoxyaceto bromoglucose.

5-Cyanophthalide is an inorganic acid that is a white solid. It has a molecular weight of 114.07 g/mol and a melting point of -43 degrees Celsius. 5-Cyanophthalide can be synthesized by reacting 5-carboxyphthalide with chlorine gas in the presence of an inert solvent and heat. The product is then purified by crystallization or recrystallization. The biological properties of 5-cyanophthalide are unknown, but it has been shown to have amide and chloride groups on either side of the molecule's carbon backbone. Mass spectrometry reveals that this compound exists as an enantiomer, meaning that it exists as two mirror images that are not superimposable on each other. This means there are two different forms: one left-handed and one right-handed form.

Please enquire for more information about 2,4-Dichlorobenzenesulphonylacetonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-(2-Cyanophenyl)-2-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-(4-Chlorobenzenesulphonyl)acetonitrile is a reactive chemical that is synthesized from chloroform and acetonitrile. It can be used to synthesize various medicines such as analgesics, muscle relaxants, and x-ray contrast agents. 2-(4-Chlorobenzenesulphonyl)acetonitrile has minimal effects on the human body and is not known to cause any major health problems. It is metabolized in the liver by oxidation of the methyl group to form 4-chlorobenzene sulfonic acid, which is excreted through urine. The chlorine atom in this molecule has a trigonal bipyramidal geometry with a bond length of 1.82 Å, which can be seen in x-ray crystallography studies.

Please enquire for more information about Boc-2-cyano-D-phenylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page

2,4,6-Trimethylbenzonitrile (TMBN) is a reactive unsaturated ketone that reacts with phosphorus pentachloride to form the corresponding chloroform. It is used in nucleophilic substitution reactions and can be hydrolyzed by hydrochloric acid to form an n-oxide. The reaction mechanism of TMBN with phosphorus pentachloride has been studied using molecular modeling and NMR spectroscopy. TMBN can be converted into an oxide, which can react with hydrogen chloride to form the corresponding chloroform. Reaction products include the 2,4,6-trichlorobenzonitrile (TCBN), which is a carcinogen.

Cyanoguanidine is an antimicrobial agent that inhibits the growth of bacteria by interfering with the synthesis of folic acid. This inhibits the production of DNA and protein, thereby leading to cell death. Cyanoguanidine has been shown to be effective in a model system for blood sampling and has been used as a pharmacological treatment for infectious diseases such as malaria. The optimum concentration for cyanoguanidine is between 5-20 mM, depending on the bacterial species. It can be synthesized from sulfamoyl chloride and dicyandiamide, which are commercially available chemicals. The analytical method for determining the inhibitory effects of cyanoguanidine on bacterial growth is plasma mass spectrometry.

Please enquire for more information about Methyl-2-isocyanoisobutyrate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Cyanomethylenetributylphosphorane (CMTP) is an agent used for the diagnosis of body formation. It is a chemical compound that can be used to produce images of tissue and organs by detecting apoptosis, or programmed cell death. CMTP binds to the glucose-dependent insulinotropic polypeptide receptor (GIPR), stimulating the release of insulin in the pancreas. CMTP also has therapeutic potential for metabolic disorders, as it has been shown to reduce triglycerides and increase HDL cholesterol levels in human serum. CMTP is synthesized from trifluoroacetic acid, which is then reacted with a cyclic peptide containing an amino acid derivative and 1-methyl-2-pyrrolidinone. This reaction produces a molecule with one free amino group at one end and two free carboxylic acid groups at the other end. The molecule can be reacted with epidermal growth factor (EGF) or insulin to

3-Cyanoethylbenzoic acid is an anthropogenic compound that is produced by the Friedel-Crafts reaction between benzoyl chloride and acrylonitrile in the presence of a base. 3-Cyanoethylbenzoic acid is used as a solvent for chromatographic methods, such as gradient elution, ion exchange, and reversed phase. 3-Cyanoethylbenzoic acid has been used to determine the optical purity of benzoate salts and amides. This compound can be taken orally in solid oral dosage form or enterically in liquid oral dosage form. 3-Cyanoethylbenzoic acid interacts with other drugs that are metabolized by CYP3A4, such as erythromycin, to produce an active metabolite (N-desmethyldesipramide).

3-Cyano-2-methylphenylboronic acid is a high quality compound that can be used as a reagent, intermediate, or building block in the synthesis of complex compounds. This chemical is also useful as a speciality chemical and research chemical. 3-Cyano-2-methylphenylboronic acid has versatile uses in organic synthesis due to its versatility in reactions and building blocks.

Ethyl 2,3-dicyanopropionate is a white crystalline solid that is soluble in organic solvents. It has the molecular formula CHClNOS and the molecular weight of 138.1 g/mol. This compound has a melting point of 92 °C and can be purchased as a mixture of cis and trans isomers. The cis form melts at 93 °C and the trans form melts at 88 °C. Ethyl 2,3-dicyanopropionate is synthesized from chlorobenzene by dehydrating it with hydrochloric acid in an organic solvent. It can also be prepared by reacting ethyl cyanoacetate with ammonia in an inert atmosphere. Impurities may include chloride, sulfoxide, or imine.