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Benzo[b]thiophen-3(2H)-one, 2-phenyl-, also known as 2-phenylbenzo[b]thiophen-3(2H)-one, is an organic compound with the molecular formula C15H10OS. It is a derivative of benzothiophenone, featuring a phenyl group attached to the 2-position of the benzothiophene core. Benzo[b]thiophen-3(2H)-one, 2-phenyl- is characterized by its aromatic structure, which includes a benzene ring fused to a thiophene ring, and a carbonyl group at the 3-position. It is a white to off-white crystalline solid and is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique chemical properties and reactivity.

53614-69-0

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53614-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53614-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53614-69:
(7*5)+(6*3)+(5*6)+(4*1)+(3*4)+(2*6)+(1*9)=120
120 % 10 = 0
So 53614-69-0 is a valid CAS Registry Number.

53614-69-0SDS

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-phenyl-1-benzothiophen-3-one

1.2 Other means of identification

Product number -
Other names 2-phenyl-benzo[b]thiophen-3-one

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:53614-69-0 SDS

53614-69-0Downstream Products

53614-69-0Relevant academic research and scientific papers

Potent, selective, and orally available benzoisothiazolone phosphomannose isomerase inhibitors as probes for congenital disorder of glycosylation Ia

Dahl, Russell,Bravo, Yalda,Sharma, Vandana,Ichikawa, Mie,Dhanya, Raveendra-Panickar,Hedrick, Michael,Brown, Brock,Rascon, Justin,Vicchiarelli, Michael,Mangravita-Novo, Arianna,Yang, Li,Stonich, Derek,Su, Ying,Smith, Layton H.,Sergienko, Eduard,Freeze, Hudson H.,Cosford, Nicholas D. P.

, p. 3661 - 3668 (2011)

We report the discovery and validation of a series of benzoisothiazolones as potent inhibitors of phosphomannose isomerase (PMI), an enzyme that converts mannose-6-phosphate (Man-6-P) into fructose-6-phosphate (Fru-6-P) and, more importantly, competes wit

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