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70499-13-7

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70499-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70499-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,9 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70499-13:
(7*7)+(6*0)+(5*4)+(4*9)+(3*9)+(2*1)+(1*3)=137
137 % 10 = 7
So 70499-13-7 is a valid CAS Registry Number.

70499-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-CHLORO-2-METHYL-4(1H)-QUINOLINONE

1.2 Other means of identification

Product number -
Other names 7-chloro-2-methyl-4-quinolone

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:70499-13-7 SDS

70499-13-7Downstream Products

70499-13-7Relevant articles and documents

Microwave-assisted Synthesis of 2-methyl-4-quinolinones via combes synthesis catalyzed by acidic resin under solvent-free condition

Yuan, Shizhen,Zhang, Kehua,Xia, Jingjing

, p. 5535 - 5538 (2013/07/26)

A simple and efficient method for the synthesis of 2-methylquinolin-4(1H)- one derivatives using NKC-9-resin as reusable eco-friendly catalyst via Combes cyclization under solvent-free and microwave irradiation conditions is described. The quinolines were obtained in high yields and in short reaction times.

Synthesis of a quinolone library from ynones

Ward, Timothy R.,Turunen, Brandon J.,Haack, Torsten,Neuenswander, Benjamin,Shadrick, William,Georg, Gunda I.

experimental part, p. 6494 - 6497 (2011/02/24)

A library of 72 quinolones was synthesized from substituted anthranilic acids, using ynone intermediates. These masked β-dicarbonyl synthons allowed cyclization under milder conditions than previously reported quinolone syntheses.

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