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4-[(5Z)-5-(3-fluorobenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]butanoic acid is a complex organic compound with the molecular formula C14H9FNO3S2. It features a 1,3-thiazolidin-3-yl core structure, which is a five-membered heterocyclic ring containing sulfur and nitrogen atoms. The compound has a 3-fluorobenzylidene group attached to the thiazolidin-3-yl ring, which contributes to its unique chemical properties. The molecule also contains a butanoic acid chain, which is a four-carbon carboxylic acid. 4-[(5Z)-5-(3-fluorobenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]butanoic acid is characterized by its Z-configuration, indicating the geometric arrangement of the double bond in the molecule. It is likely to be used in pharmaceutical or chemical research due to its specific structural features, which may confer particular biological activities or reactivity.

5755-76-0

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5755-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5755-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5755-76:
(6*5)+(5*7)+(4*5)+(3*5)+(2*7)+(1*6)=120
120 % 10 = 0
So 5755-76-0 is a valid CAS Registry Number.

5755-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoethyl tosylate

1.2 Other means of identification

Product number -
Other names 2-(4-Methylphenylsulfonyl)-ethylbromid

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:5755-76-0 SDS

5755-76-0Relevant academic research and scientific papers

Metal-free visible-light-promoted C(sp3)-H functionalization of aliphatic cyclic ethers using trace O2

Blackburn, Bryan G.,Cooke, Maria Victoria,Laulhé, Sébastien,Niu, Ben,Sachidanandan, Krishnakumar

, p. 9454 - 9459 (2021/12/09)

Presented is a light-promoted C-C bond forming reaction yielding sulfone and phosphate derivatives at room temperature in the absence of metals or photoredox catalyst. This transformation proceeds in neat conditions through an auto-oxidation mechanism which is maintained through the leaching of trace amounts of O2 as sole green oxidant. This journal is

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