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1H-Benzimidazole, 5-chloro-2-cyclopropyl-(9CI) is a chemical compound with the molecular formula C9H9ClN2. It belongs to the class of benzimidazoles, which are heterocyclic compounds containing a benzene ring fused to an imidazole ring. This specific compound features a 5-chloro substituent and a 2-cyclopropyl group, which are attached to the benzimidazole core. The presence of the chlorine atom and cyclopropyl group can influence the compound's reactivity, solubility, and potential applications in various chemical and pharmaceutical processes. Due to its unique structure, 1H-Benzimidazole, 5-chloro-2-cyclopropyl-(9CI) may be used as an intermediate in the synthesis of more complex molecules or as a building block in the development of new drugs and materials.

4887-92-7

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4887-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4887-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4887-92:
(6*4)+(5*8)+(4*8)+(3*7)+(2*9)+(1*2)=137
137 % 10 = 7
So 4887-92-7 is a valid CAS Registry Number.

4887-92-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-2-cyclopropyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names oxypyrimidine-4-carboxylic

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4887-92-7 SDS

4887-92-7Downstream Products

4887-92-7Relevant academic research and scientific papers

Catalyst free approach to benzimidazoles using air as the oxidant at room temperature

Zhang, Chun,Zhang, Liangren,Jiao, Ning

supporting information, p. 3273 - 3276 (2013/01/16)

A green and practical method to construct benzimidazoles, which are ubiquitous structural units in a number of biologically active compounds, has been developed. The catalyst and additive free conditions, using air as oxidant and the mild conditions make

NITRATION DE BENZIMIDAZOLES SUBSTITUES

Benchidmi, M.,Kihel, A. El,Essassi, E. M.,Knouzi, N.,Toupet, L.,et al.

, p. 605 - 612 (2007/10/02)

The mononitration of some 2-Alkyl-5(6)chloro-(or methyl-)benzimidazoles was carried out because the chemical literature results were ambiguous.Our work has shown that the nitro group was introduced in 6 (or 5) position.

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