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214337-39-0

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214337-39-0 Usage

General Description

2-Bromo-5-methoxy-benzothiazole (9CI) is a chemical compound that belongs to the family of thiazoles and derivatives, specifically the class of benzothiazoles. It contains a benzothiazole ring which is further substituted by a bromo group at the 2nd position and a methoxy group at the 5th position. Due to its chemical structure, this substance is potentially involved in various biological and chemical interactions, implying it could be used in several scientific fields, like medicinal chemistry for drug discovery. Its specific properties, uses, and potential hazards need proper investigation to ensure safe and effective utilization in any applied context.

Check Digit Verification of cas no

The CAS Registry Mumber 214337-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,3,3 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 214337-39:
(8*2)+(7*1)+(6*4)+(5*3)+(4*3)+(3*7)+(2*3)+(1*9)=110
110 % 10 = 0
So 214337-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6BrNOS/c1-11-5-2-3-7-6(4-5)10-8(9)12-7/h2-4H,1H3

214337-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-5-methoxy-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-Bromo-5-methoxybenzothiazole

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:214337-39-0 SDS

214337-39-0Relevant articles and documents

Design and synthesis of 5,6-fused heterocyclic amides as Raf kinase inhibitors

Ramurthy, Savithri,Aikawa, Mina,Amiri, Payman,Costales, Abran,Hashash, Ahmad,Jansen, Johanna M.,Lin, Song,Ma, Sylvia,Renhowe, Paul A.,Shafer, Cynthia M.,Subramanian, Sharadha,Sung, Leonard,Verhagen, Joelle

supporting information; experimental part, p. 3286 - 3289 (2011/06/24)

Two scaffolds based on 5,6-fused heterocyclic backbones were designed and synthesized as Raf kinase inhibitors. The scaffolds were assessed for in vitro pan-Raf inhibition, activity in cell proliferation and target modulation assays, and pharmacokinetic p

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