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2-(2-Bromophenyl)thiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30216-46-7

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30216-46-7 Usage

Structure

A thiazole derivative with a bromophenyl group attached to the second carbon atom of the thiazole ring.

Potential applications

Pharmaceutical industry (building block for synthesis of biologically active compounds), material science (development of new materials with specific properties), and agrochemical industry (development of new pesticides or herbicides).

Need for further research

To explore its potential applications and properties in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 30216-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30216-46:
(7*3)+(6*0)+(5*2)+(4*1)+(3*6)+(2*4)+(1*6)=67
67 % 10 = 7
So 30216-46-7 is a valid CAS Registry Number.

30216-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-bromophenyl)-1,3-thiazole

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:30216-46-7 SDS

30216-46-7Downstream Products

30216-46-7Relevant academic research and scientific papers

Synthesis of iodinated thiazolo[2,3-a]isoquinolinium salts and their crystal structures with/without halogen bond

Matsumoto, Shoji,Sumida, Ryuta,Tan, Sia Er,Akazome, Motohiro

, p. 755 - 775 (2019/04/26)

We investigated the cyclization reaction of 2-(2-(phenylethynyl)-phenyl)thiazoles with I2. A six-membered ring was formed to produce the corresponding thiazolo[2,3-a]isoquinolin-7-ium salts. The counter anions (I? and I3?) varied bas

ARYLSULFONYL BENZYL ETHERS AS 5-HT2A ANTAGONISTS

-

Page/Page column 20, (2010/11/23)

Compounds of formula (I) are potent and selective antagonists of the 5-HT2A receptor, and hence are useful in treatment of various CNS disorders.

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