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80567-65-3

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80567-65-3 Usage

General Description

2(3H)-Benzothiazolone,6-hydroxy-(9CI) is a chemical compound with the molecular formula C7H5NO2S. It is a benzothiazolone derivative with a hydroxyl group attached to the sixth carbon of the molecule. 2(3H)-Benzothiazolone,6-hydroxy-(9CI) is used in the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also known for its biological activities and is studied for its potential medicinal properties. The chemical structure of 2(3H)-Benzothiazolone,6-hydroxy-(9CI) makes it a versatile building block for the development of various compounds with potential applications in medicine and chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 80567-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80567-65:
(7*8)+(6*0)+(5*5)+(4*6)+(3*7)+(2*6)+(1*5)=143
143 % 10 = 3
So 80567-65-3 is a valid CAS Registry Number.

80567-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-3H-1,3-benzothiazol-2-one

1.2 Other means of identification

Product number -
Other names 6-hydroxy-3H-benzothiazol-2-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:80567-65-3 SDS

80567-65-3Relevant articles and documents

Inhibitors of cyclic AMP phosphodiesterase. 1. Analogues of cilostamide and anagrelide

Jones,Venuti,Alvarez,Bruno,Berks,Prince

, p. 295 - 303 (2007/10/02)

Evaluation of a series of lactam heterocyclic analogues of cilostamide as inhibitors of cyclic AMP phosphodiesterase derived from both human platelets and rat heart in comparison with their corresponding methoxy-substituted heterocycles has revealed that the N-cyclohexyl-N-methyl-4-oxybutyramide side chain of 2 is an important lipophilic and/or steric pharmacophore. Attachment of this side chain to the parent heterocycle of the potent cyclic AMP phosphodiesterase inhibitor anagrelide afforded the hybrid structure RS-82856, shown to be more potent than either of its progenitors as an inhibitor of cyclic AMP phosphodiesterase or of ADP-induced platelet aggregation. The available in vitro data suggest that 1 possesses potentially useful antithrombotic and cardiotonic properties.

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