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93202-42-7

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93202-42-7 Usage

Compound type

Heterocyclic compound

Core structure

Benzimidazole

Functional group

Carbonyl group attached to the third carbon atom

Potential uses

Various research and industrial applications

Safety precautions

Safe handling and storage procedures should be followed to prevent hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 93202-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,0 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93202-42:
(7*9)+(6*3)+(5*2)+(4*0)+(3*2)+(2*4)+(1*2)=107
107 % 10 = 7
So 93202-42-7 is a valid CAS Registry Number.

93202-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-propionylbenzimidazolin-2-one

1.2 Other means of identification

Product number -
Other names 5-Propionyl-1,3-dihydro-benzoimidazol-2-one

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:93202-42-7 SDS

93202-42-7Downstream Products

93202-42-7Relevant articles and documents

FRIDEL-CRAFTS ACYLATION OF BENZIMIDAZOLIN-2-ONES WITH ALIPHATIC ACID CHLORIDES

Kadyrov, Ch. Sh.,Khalikov, S. S.

, p. 658 - 661 (1984)

The acylation of benzimidazolin-2-one and its 5,6-disubstituted derivatives with aliphatic acid chlorides in the presence of anhydrous aluminium chloride was studied.The corresponding 5(6)-acyl-, 5-R-6-acyl, and 5,6-dimethyl-4-acylbenzimidazolin-2-ones, the structures of which were confirmed by the results of elementary analysis and IR, PMR, and mass spectroscopy, were obtained.The yields of the acylation products depend on the electronic effects of the substituents in the benzene ring of the benzimidazolin-2-one on steric factors.

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