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872726-34-6

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872726-34-6 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 49, p. 179, 2006 DOI: 10.1021/jm050942k

Check Digit Verification of cas no

The CAS Registry Mumber 872726-34-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,7,2 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 872726-34:
(8*8)+(7*7)+(6*2)+(5*7)+(4*2)+(3*6)+(2*3)+(1*4)=196
196 % 10 = 6
So 872726-34-6 is a valid CAS Registry Number.

872726-34-6SDS

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 5-fluoro-2-(4-methoxyphenyl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names -

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:872726-34-6 SDS

872726-34-6Downstream Products

872726-34-6Relevant articles and documents

Synthesis of 2-substituted benzothiazoles from 1-iodo-2-nitrobenzenes by a copper-catalyzed one-pot three-component reaction

Liu, Jidan,Gui, Qingwen,Yang, Zhiyong,Tan, Ze,Guo, Ruqing,Shi, Ji-Cheng

, p. 943 - 951 (2013/05/08)

A novel method was developed for synthesizing 2-substituted 1,3-benzothiazoles through a copper-catalyzed, one-pot, three-component reaction of a 1-iodo-2-nitrobenzene with sodium sulfide and an aldehyde. Georg Thieme Verlag Stuttgart - New York.

2-Arylbenzothiazole derivatives

-

Page/Page column 9, (2008/06/13)

A compound of general structure I, wherein the compound is optionally in the form of an N-oxide or S-oxide or prodrug form and/or pharmaceutically acceptable salt thereof wherein: each of R1 to R9 is independently selected from hydro

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