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88346-57-0

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88346-57-0 Usage

Heterocyclic compound

Containing an imidazole ring The compound has a ring structure in its molecular structure, specifically an imidazole ring, which consists of a 5-membered ring with three carbon atoms and two nitrogen atoms.

Carbonitrile group

A cyano group (C≡N) attached to the imidazole ring This is a functional group present in the compound, consisting of a carbon atom triple-bonded to a nitrogen atom.

4-methyl-2-phenyl substituent

A phenyl group attached to the imidazole ring at position 2, with a methyl group (CH3) attached at position 4 This describes the specific arrangement of the substituents on the imidazole ring, which can influence the compound's properties and reactivity.

Potential applications

Pharmaceutical and agrochemical industries Due to its biological activities, 1H-Imidazole-1-carbonitrile, 4-methyl-2-phenylmay be used in the development of drugs and agrochemicals.

Biological activities

Antifungal and antibacterial properties The compound exhibits these activities, which can be useful in treating infections and protecting crops from diseases.

Building block in synthesis

Used in the synthesis of various pharmaceuticals and fine chemicals 1H-Imidazole-1-carbonitrile, 4-methyl-2-phenylcan be used as a starting material or intermediate in the production of other compounds.

Coordination chemistry

Potential as a ligand due to the presence of the nitrogen-containing imidazole ring The compound may form coordination complexes with metal ions, which can be useful in various applications, such as catalysis and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 88346-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,4 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88346-57:
(7*8)+(6*8)+(5*3)+(4*4)+(3*6)+(2*5)+(1*7)=170
170 % 10 = 0
So 88346-57-0 is a valid CAS Registry Number.

88346-57-0Upstream product

88346-57-0Downstream Products

88346-57-0Relevant articles and documents

Synthesis of Some Alkyl- and Arylimidazoles

Watanabe, T.,Nishiyama, J.,Hirate, R.,Uehara, K.,Inoue, M.,et al.

, p. 1277 - 1281 (2007/10/02)

The pyrolysis of 2-azidopyrazines led to give 1-cyanoimidazoles, which were hydrolyzed in alkaline and acidic media to the corresponding imidazoles.This ring transformation occured also by photolysis.

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