Welcome to LookChem.com Sign In|Join Free
  • or
5-chloro-3-(4-chlorophenyl)-1-methyl-benzoimidazol-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79759-66-3

Post Buying Request

79759-66-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

79759-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79759-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,5 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79759-66:
(7*7)+(6*9)+(5*7)+(4*5)+(3*9)+(2*6)+(1*6)=203
203 % 10 = 3
So 79759-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H10Cl2N2O/c1-17-12-7-4-10(16)8-13(12)18(14(17)19)11-5-2-9(15)3-6-11/h2-8H,1H3

79759-66-3SDS

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-3-(4-chlorophenyl)-1-methylbenzimidazol-2-one

1.2 Other means of identification

Product number -
Other names 1,3-Dihydro-5-chloro-3-(4-chlorophenyl)-1-methyl-2H-benzimidazol-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:79759-66-3 SDS

79759-66-3Downstream Products

79759-66-3Relevant academic research and scientific papers

Method for preparing benzimidazolone by electro-catalysis

-

Paragraph 0038-0042; 0053-0057, (2021/07/31)

The invention discloses a method for preparing benzimidazolone through electro-catalysis. The method comprises the following steps: dissolving trisubstituted phenyl urea in a three-necked flask filledwith an organic solvent, inserting a Pt electrode as a

Catalyst-Free Electrosynthesis of Benzimidazolones through Intramolecular Oxidative C?N Coupling

Li, Jiang-Sheng,Yang, Pan-Pan,Xie, Xin-Yun,Jiang, Si,Tao, Li,Li, Zhi-Wei,Lu, Cui-Hong,Liu, Wei-Dong

supporting information, p. 1977 - 1981 (2020/04/20)

The electrochemical synthesis of N, N’-disubstituted benzimidazolones from ureas through an intramolecular anodic dehydrogenative N?H/C?H coupling has been developed. The reaction undergoes under the undivided electrolysis conditions and obviates the need for any catalysts and chemical oxidants. (Figure presented.).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 79759-66-3