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67521-01-1

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67521-01-1 Usage

Chemical compound

2H-Benzimidazol-2-one,5-acetyl-1,3-dihydro-6-methyl-(9CI)

Type

Heterocyclic compound

Structure

Benzimidazole core structure

Use

Building block for synthesis of pharmaceuticals and agrochemicals

Applications

Development of drugs for cancer, infectious diseases, and CNS disorders

Versatility

Useful in medicinal chemistry research and drug development

Synthetic versatility

Important target for further studies in organic and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 67521-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67521-01:
(7*6)+(6*7)+(5*5)+(4*2)+(3*1)+(2*0)+(1*1)=121
121 % 10 = 1
So 67521-01-1 is a valid CAS Registry Number.

67521-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetyl-6-methyl-1,3-dihydrobenzimidazol-2-one

1.2 Other means of identification

Product number -
Other names 5-acetyl-6-methyl-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:67521-01-1 SDS

67521-01-1Downstream Products

67521-01-1Relevant articles and documents

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

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

, p. 658 - 661 (2007/10/02)

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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