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2735-61-7

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2735-61-7 Usage

General Description

(1-Methyl-1H-benzoimidazol-2-yl)-acetic acid ethyl ester is a chemical compound that belongs to the class of benzoimidazole derivatives. It is a derivative of benzoimidazole and acetic acid, with an ethyl ester functional group. (1-Methyl-1H-benzoimidazol-2-yl)-acetic acid ethyl ester may have potential pharmacological properties due to its structural features and may be used in pharmaceutical research and development. It is important to handle this chemical with caution, as it may have specific hazards and risks associated with its handling and use. Overall, further research and investigation may be needed to fully understand the properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 2735-61-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2735-61:
(6*2)+(5*7)+(4*3)+(3*5)+(2*6)+(1*1)=87
87 % 10 = 7
So 2735-61-7 is a valid CAS Registry Number.

2735-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(1-methylbenzimidazol-2-yl)acetate

1.2 Other means of identification

Product number -
Other names 2-Benzimidazoleaceticacid,1-methyl-,ethyl ester (7CI,8CI)

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:2735-61-7 SDS

2735-61-7Relevant articles and documents

Synthesis and photochromic properties of 2-(3-nitro-2-pyridylmethyl)benzazoles

Zakhs,Ponyaev,Subbotina,El'tsov

, p. 1076 - 1087 (2007/10/03)

2-(3-Nitro-2-pyridylmethyl)benzazoles were synthesized, and their photochromic properties were studied by flash photolysis. Introduction of a nitropyridyl instead of the nitrophenyl moiety into the 2-methyl group insignificantly increases the basicity of the methylene group. Nitropyridyl-substituted benzazoles give rise to three detectable photoinduced forms: the corresponding union at pH > 10, azamerocyanine at pH ≈ 4, and monomethinecyanine at pH ≈ 1. Irradiation of solutions of weakly basic henzoxazole and benzothiazole derivatives at pH ≈ 4 results in formation of neutral chelate structures in which the hydrogen atom is linked simultaneously to two nitrogen atoms: one in the pyridine ring, and the second, in the azole ring.

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