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70374-27-5

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70374-27-5 Usage

Chemical structure

Thieno-thiazine ring system with a chloro and hydroxyl group attached, as well as a pyridine substituent

Activity

Potent and selective antagonist of the dopamine D3 receptor

Potential therapeutic uses

Treatment of neurological disorders such as schizophrenia and drug addiction

Importance

Unique structure and functional properties make it an important target for pharmaceutical research and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 70374-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70374-27:
(7*7)+(6*0)+(5*3)+(4*7)+(3*4)+(2*2)+(1*7)=115
115 % 10 = 5
So 70374-27-5 is a valid CAS Registry Number.

70374-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-4-hydroxy-2-methyl-1,1-dioxo-1,2-dihydro-1λ6-thieno[3,2-e][1,2]thiazine-3-carboxylic acid pyridin-2-ylamide

1.2 Other means of identification

Product number -
Other names 6-chloro-4-hydroxy-2-methyl-3-(2-pyridyl-carbamoyl)-2H-thieno[3,2-e]-1,2-thiazine-1,1-dioxide

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:70374-27-5 SDS

70374-27-5Downstream Products

70374-27-5Relevant articles and documents

Thiazine derivatives

-

, (2008/06/13)

Anti-inflammatory, analgesic, anti-rheumatic and anti-thrombotic thienothiazine derivatives having the formula STR1 wherein A together with the two carbon atoms forms the group STR2 and the dotted line indicates the double bond present in the first and last thieno structures above, R1 is lower alkyl, R2 is the radical of an aromatic heterocycle with 1 to 4 hetero atoms optionally substituted by one or two lower alkyl groups, or a phenyl radical optionally substituted by halogen, hydroxy, lower alkyl, trifluoromethyl or lower alkoxy, R3 is halogen and R3' is hydrogen or halogen, and pharmaceutically acceptable salts thereof are described.

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