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123895-42-1

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123895-42-1 Usage

General Description

2-(bromomethyl)-5-(trifluoromethyl) benzothiazole is a chemical compound with the molecular formula C9H5BrF3NS. It is a benzothiazole derivative with a bromine atom and a trifluoromethyl group attached to the benzene ring. 2-(BROMOMETHYL)-5-(TRIFLUOROMETHYL) BENZOTHIAZOLE is used in the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential applications in the development of organic light-emitting diodes (OLEDs) and as a fluorescent probe for the detection of metal ions in biological systems. Additionally, it has been investigated for its antimicrobial and anti-cancer properties. The compound's unique structure and properties make it a versatile building block in organic synthesis and a target for further research in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 123895-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,9 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123895-42:
(8*1)+(7*2)+(6*3)+(5*8)+(4*9)+(3*5)+(2*4)+(1*2)=141
141 % 10 = 1
So 123895-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H5BrF3NS/c10-4-8-14-6-3-5(9(11,12)13)1-2-7(6)15-8/h1-3H,4H2

123895-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(bromomethyl)-5-(trifluoromethyl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-bromomethyl-5-trifluoromethyl-benzothiazole

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:123895-42-1 SDS

123895-42-1Downstream Products

123895-42-1Relevant articles and documents

Highly selective aldose reductase inhibitors. II. Optimization of the aryl part of 3-(arylmethyl)-2,4,5-trioxoimidazolidine-1-acetic acids

Kotani, Takayuki,Ishii, Akira,Nagaki, Yasuhiro,Toyomaki, Yoshio,Yago, Hisashi,Suehiro, Seishi,Okukado, Nobuhisa,Okamoto, Kaoru

, p. 297 - 304 (2007/10/03)

Accumulation of intracellular sorbitol, the product of glucose reduction catalyzed by aldose reductase (AR) [EC 1.1.1.21], is thought to be the main culprit in the development of diabetic complications. A series of 3- arylalkyl-2,4,5-trioxoimidazolidine-1-acetic acids was prepared and tested for inhibitory activities towards AR and aldehyde reductase (ALR) [EC 1.1.1.2]. These derivatives showed strong inhibitory activity against AR without markedly inhibiting ALR. In particular, the compounds with 3- nitrophenyl, 4-chloro-3-nitrophenyl, and chloro-substituted benzothiazolyl groups as the aryl part showed powerful AR-inhibitory activity. The chloro- substituted benzothiazolyl compound showed an AR selectivity of more than 5000 fold.

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