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6306-71-4

6306-71-4

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6306-71-4 Usage

Uses

Ethyl (1H-Benzo[d]imidazol-2-yl)carbamate is used in method of making 1-(Acyloxy)-alkyl Carbamate prodrugs of amine containing drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 6306-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6306-71:
(6*6)+(5*3)+(4*0)+(3*6)+(2*7)+(1*1)=84
84 % 10 = 4
So 6306-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O2/c1-2-15-10(14)13-9-11-7-5-3-4-6-8(7)12-9/h3-6H,2H2,1H3,(H2,11,12,13,14)

6306-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(1H-benzimidazol-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names Ethyl 2-benzimidazolecarbamate

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:6306-71-4 SDS

6306-71-4Downstream Products

6306-71-4Relevant articles and documents

CRYSTAL AND MOLECULAR STRUCTURE OF N-(2-BENZIMIDAZOLYL)-O-ALKYL CARBAMATES

Sokol, V. I.,Davidov, V. V.,Porai-Koshits, M. A.,Zaitsev, B. E.,Palishkin, M. V.,et al.

, p. 1148 - 1153 (1988)

-

Phosphonium-mediated cyclization of N-(2-aminophenyl)thioureas: Efficient synthesis of 2-aminobenzimidazoles

Wan, Zhao-Kui,Ousman, Erena Farah,Papaioannou, Nikolaos,Saiah, Eddine

supporting information; experimental part, p. 4149 - 4152 (2011/09/19)

BOP efficiently promoted the phosphonium-mediated cyclization of thioureas, leading to a convenient synthesis of 2-aminobenzimidazoles. Compared to conventional methods, the reactions were complete at room temperature with times ranging from a few minutes

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