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153568-04-8

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153568-04-8 Usage

General Description

AKOS B018372 is a chemical compound that is also known as 4'-Hydroxy-5-methoxyacetophenone. It is a derivative of acetophenone, which is a white solid with a sweet, flowery odor. AKOS B018372 is commonly used in the synthesis of pharmaceuticals and organic compounds. It has also been researched for its potential antioxidant and anti-inflammatory properties. Additionally, it has been studied for its potential as a natural colorant in the food and cosmetic industries. Overall, AKOS B018372 is a versatile compound with a wide range of potential industrial and medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 153568-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,5,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153568-04:
(8*1)+(7*5)+(6*3)+(5*5)+(4*6)+(3*8)+(2*0)+(1*4)=138
138 % 10 = 8
So 153568-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H6F3NOS2/c12-11(13,14)7-4-2-1-3-6(7)5-8-9(16)15-10(17)18-8/h1-5H,(H,15,16,17)/b8-5+

153568-04-8SDS

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 (5E)-2-Mercapto-5-[2-(trifluoromethyl)benzylidene] -1,3-thiazol-4(5H)-one

1.2 Other means of identification

Product number -
Other names AKOS B018372

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:153568-04-8 SDS

153568-04-8Downstream Products

153568-04-8Relevant articles and documents

Synthesis and antifungal activity of (Z)-5-arylidenerhodanines

Sortino, Maximiliano,Delgado, Paula,Juarez, Sabina,Quiroga, Jairo,Abonia, Rodrigo,Insuasty, Braulio,Nogueras, Manuel,Rodero, Laura,Garibotto, Francisco M.,Enriz, Ricardo D.,Zacchino, Susana A.

, p. 484 - 494 (2007)

An efficient microwave-assisted synthesis of new (Z)-5-arylidenerhodanines under solvent-free conditions is described and their in vitro antifungal activity was evaluated following the CLSI (formerly NCCLS) guidelines against a panel of both standardized

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