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3-(1,3-benzothiazol-2-yl)-4-{4-[(1-methyl-1H-imidazol-2-yl)sulfanyl]-3-nitrophenyl}but-3-enoic acid is a complex organic compound with a molecular formula of C21H14N4O4S3. It is characterized by the presence of a benzothiazole ring, an imidazole ring, and a butenoic acid group. The compound features a 3-nitrophenyl group connected to the imidazole ring through a sulfanyl bridge. This chemical structure is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique electronic and steric properties. The compound's specific arrangement of functional groups and heterocycles can influence its reactivity, stability, and potential interactions with biological targets, making it a subject of interest for researchers in the development of new drugs and materials.

5487-84-3

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5487-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5487-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,8 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5487-84:
(6*5)+(5*4)+(4*8)+(3*7)+(2*8)+(1*4)=123
123 % 10 = 3
So 5487-84-3 is a valid CAS Registry Number.

5487-84-3SDS

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 3-(1,3-benzothiazol-2-yl)-4-[4-(1-methylimidazol-2-yl)sulfanyl-3-nitrophenyl]but-3-enoic acid

1.2 Other means of identification

Product number -
Other names (BC2H5N(4-Br-C6H4))3

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:5487-84-3 SDS

5487-84-3Upstream product

5487-84-3Downstream Products

5487-84-3Relevant academic research and scientific papers

Borazines stable to hydrolysis

Nagasawa, Koichiro

, p. 442 - 445 (2007/10/06)

In order to evaluate the steric effect of increasing the stability of the borazine ring, B-tri-2,6-xylyl- and B-trimesityl-N-trimethylborazine were prepared and subjected to Friedel-Crafts acetylation, free-radical bromination, and hydrolysis experiments.

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