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3-bromo-7-methylquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66438-79-7

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66438-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66438-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,3 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66438-79:
(7*6)+(6*6)+(5*4)+(4*3)+(3*8)+(2*7)+(1*9)=157
157 % 10 = 7
So 66438-79-7 is a valid CAS Registry Number.

66438-79-7SDS

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 3-bromo-7-methylquinoline

1.2 Other means of identification

Product number -
Other names 3-bromo-7-methyl-quinoline

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:66438-79-7 SDS

66438-79-7Upstream product

66438-79-7Relevant academic research and scientific papers

Synthesis and antibacterial activity of novel ketolides with 11,12-quinoylalkyl side chains

Zhao, Zhe-hui,Zhang, Xiao-xi,Jin, Long-long,Yang, Shuang,Lei, Ping-sheng

supporting information, p. 2358 - 2363 (2018/06/25)

A series of quinoylalkyl side chains was designed and synthesized, followed by introduction into ketolides by coupling with building block 6 or 32. The corresponding targets 7a–n, 33b, and 33e were tested for their in vitro activities against a series of macrolide-sensitive and macrolide-resistant pathogens. Some of them showed a similar antibacterial spectrum and comparable activity to telithromycin. Among them, two C2-F ketolides, compounds 33b and 33e, displayed excellent activities against macrolide-sensitive and macrolide-resistant pathogens.

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