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412923-40-1

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412923-40-1 Usage

General Description

2-Bromothiazolo[5,4-b]pyridine is a unique chemical compound belonging to the class of organoheterocyclic compounds known as thiazolopyridines. These are aromatic compounds featuring a thiazolopyridine moiety, which is a six-member ring made up of a pyridine fused to a thiazole. The molecular formula of 2-Bromothiazolo[5,4-b]pyridine is C7H4BrN2S. It has a molar mass of 230.089 g/mol. Due to its chemical structure, this compound may have various applications in the field of organic chemistry, such as serving as a reagent or intermediate in the synthesis of other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 412923-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,9,2 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 412923-40:
(8*4)+(7*1)+(6*2)+(5*9)+(4*2)+(3*3)+(2*4)+(1*0)=121
121 % 10 = 1
So 412923-40-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrN2S/c7-6-9-4-2-1-3-8-5(4)10-6/h1-3H

412923-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromothiazolo[5,4-b]pyridine

1.2 Other means of identification

Product number -
Other names 2-bromo-[1,3]thiazolo[5,4-b]pyridine

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:412923-40-1 SDS

412923-40-1Relevant articles and documents

Design, synthesis, and biological activity of novel factor Xa inhibitors: Improving metabolic stability by S1 and S4 ligand modification

Komoriya, Satoshi,Kobayashi, Shozo,Osanai, Ken,Yoshino, Toshiharu,Nagata, Tsutomu,Haginoya, Noriyasu,Nakamoto, Yumi,Mochizuki, Akiyoshi,Nagahara, Takayasu,Suzuki, Makoto,Shimada, Takashi,Watanabe, Kengo,Isobe, Yumiko,Furugoori, Taketoshi

, p. 1309 - 1330 (2006)

Serine protease factor xa (fXa) inhibitor 1 showed good ex vivo anti-fXa activity upon oral administration in rats. However, it has been revealed that 1 had low metabolic stability against human liver microsomes. To improve the metabolic stability, we att

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