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3-(5-methyl-1H-benzo[d]imidazol-2-yl)quinolin-2(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

335672-04-3

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335672-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335672-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,6,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 335672-04:
(8*3)+(7*3)+(6*5)+(5*6)+(4*7)+(3*2)+(2*0)+(1*4)=143
143 % 10 = 3
So 335672-04-3 is a valid CAS Registry Number.

335672-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5-methyl-1H-benzo[d]imidazol-2-yl)quinolin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 3-(5-Methyl-benzoimidazol-2-yl)-quinolin-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:335672-04-3 SDS

335672-04-3Downstream Products

335672-04-3Relevant academic research and scientific papers

A simple one-pot synthesis of new imidazol-2-yl-lh-quinolin-2-ones from the direct reaction of 2-chloroquinolin-3-carbaldehyde with aromatic o-diamines

Abonia, Rodrigo,Castillo, Juan,Cuervo, Paola,Insuasty, Braulio,Quiroga, Jairo,Ortiz, Alejandro,Nogueras, Manuel,Cobo, Justo

, p. 317 - 325 (2010)

An alternative and general one-pot synthesis of a library of novel imidazol-2-yl-1H-quinolin-2-one derivatives was performed in 70 % aqueous acetic acid by the direct reaction of 2-chloroquinolin-3-carbaldehyde with aromatic o-diamines. Experiments showed that adding Amberlyst (20% w/w) to the reaction media increased both the speed of reaction as well as the yield of products. Both DFT theoretical calculations and X-ray diffraction studies confirmed the proposed structures and the more stable conformation of the obtained products, Antitumor studies against sixty different cancer cell lines showed the potential of these kinds of compounds.

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