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75219-13-5

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75219-13-5 Usage

Structure

A derivative of benzothiazole, containing a benzene ring fused to a thiophene ring

Appearance

Yellowish crystalline powder

Usage

Commonly used in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals

Potential applications

In materials science and as a fluorescent dye

Biological activities

Antimicrobial, antioxidant, and anti-inflammatory properties, making it a target for research in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 75219-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,1 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75219-13:
(7*7)+(6*5)+(5*2)+(4*1)+(3*9)+(2*1)+(1*3)=125
125 % 10 = 5
So 75219-13-5 is a valid CAS Registry Number.

75219-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,3-benzothiazol-2-ylsulfanyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names HMS1481N20

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:75219-13-5 SDS

75219-13-5Relevant articles and documents

Esterase-sensitive sulfur dioxide prodrugs inspired by modified Julia olefination

Wang, Wenyi,Wang, Binghe

supporting information, p. 10124 - 10127 (2017/09/23)

Sulfur dioxide (SO2) is an endogenously produced gaseous molecule, and is emerging as a potential gasotransmitter. Herein, we describe the first series of esterase-sensitive prodrugs inspired by modified Julia olefination as SO2 donors.

Conformations of 2-alkyl(aryl)thiocyclohexanones

Samoshin,Kudryavtsev,Yartseva,Lutsenko,Zefirov

, p. 1279 - 1281 (2007/10/03)

According to the 1H NMR data, 2-alkyl(aryl)thiocyclohexanones exist mainly as axial conformers. An exception is 2-(2-benzothiazolylthio)cyclohexanone which exists mainly as equatorial conformer due to intramolecular electrostatic interactions.

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