cas 4414-88-4|| where to buy 1H-Benzimidazole-2-acetonitrile

Product Name:1H-Benzimidazole-2-acetonitrile

IUPAC Name:2-(1H-1,3-benzodiazol-2-yl)acetonitrile

: CAS：4414-88-4; Molecular Formula：C9H7N3; Purity：98%

: Catalog Number：CM157812; Molecular Weight：157.18

Packing Unit	Available Stock	Price($)
CM157812-100g	in stock	ƏƏř
CM157812-500g	in stock	Žǎƴ

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Product Details

: CAS NO:4414-88-4; Molecular Formula:C9H7N3; Melting Point:-; Smiles Code:C1=CC=CC2=C1[NH]C(=N2)CC#N; Density:

: Catalog Number:CM157812; Molecular Weight:157.18; Boiling Point:439.5°C at 760 mmHg; MDL No:MFCD00005601; Storage:Store at room temperature.

Category Infos

: Benzimidazoles; Benzimidazole is a benzo derivative of imidazole. It is a kind of bicyclic aromatic organic compounds, which is formed by fusing a six-membered benzene ring and five-membered imidazole at positions 4 and 5 of imidazole ring. It is an important pharmacophore of many biologically active heterocyclic compounds with various pharmacological activities. Benzimidazoles and their derivatives have developed into dynamic heterocyclic systems due to their potency in a variety of biologically active compounds such as anticancer, bactericidal and antiviral drugs. Benzimidazoles are a class of therapeutic motifs with broad relevance in medicinal chemistry.

Product Other Information

Product Overview	1H-Benzimidazole-2-acetonitrile (BZCN) is an organic compound belonging to the benzimidazole family, which is widely used in a variety of scientific research applications. It is highly soluble in water and has a wide variety of uses in organic synthesis and drug development. BZCN is a versatile compound that has been used in a number of different scientific research applications.
Synthesis and Application	The synthesis of 1H-Benzimidazole-2-acetonitrile is relatively simple. It can be synthesized from 1H-benzimidazole and acetonitrile in the presence of an acid catalyst. The reaction takes place in a two-step process. First, the 1H-benzimidazole is converted to an acetonitrile adduct with the help of an acid catalyst. The second step involves the deprotonation of the acetonitrile adduct, which results in the formation of 1H-Benzimidazole-2-acetonitrile. 1H-Benzimidazole-2-acetonitrile has been widely used in a variety of scientific research applications. It has been used to study the biochemical and physiological effects of different compounds. In addition, 1H-Benzimidazole-2-acetonitrile has been used to study the pharmacodynamics of different compounds.
Future Directions	The use of 1H-Benzimidazole-2-acetonitrile in scientific research is still in its infancy, and there are a number of potential future directions for its use. One potential future direction is the use of 1H-Benzimidazole-2-acetonitrile in drug development. 1H-Benzimidazole-2-acetonitrile could be used to develop new drugs that target specific receptors in the body. In addition, 1H-Benzimidazole-2-acetonitrile could be used to develop new drugs that target specific diseases or conditions. Another potential future direction for 1H-Benzimidazole-2-acetonitrile is the use of 1H-Benzimidazole-2-acetonitrile in the development of new diagnostic tests. 1H-Benzimidazole-2-acetonitrile could be used to develop new tests that can detect the presence of certain compounds in the body. Finally, 1H-Benzimidazole-2-acetonitrile could be used to develop new treatments for various diseases or conditions.