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10202-40-1

10202-40-1

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10202-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10202-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,0 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10202-40:
(7*1)+(6*0)+(5*2)+(4*0)+(3*2)+(2*4)+(1*0)=31
31 % 10 = 1
So 10202-40-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H24F3N3OS2/c21-20(22,23)15-2-3-18-17(14-15)26(16-4-13-28-19(16)29-18)6-1-5-24-7-9-25(10-8-24)11-12-27/h2-4,13-14,27H,1,5-12H2

10202-40-1SDS

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-[4-[3-[6-(trifluoromethyl)thieno[2,3-b][1,4]benzothiazin-4-yl]propyl]piperazin-1-yl]ethanol

1.2 Other means of identification

Product number -
Other names Flutizenol

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:10202-40-1 SDS

10202-40-1Downstream Products

10202-40-1Relevant articles and documents

Synthesis of Isomeric Thienobenzothiazines and Their Effect on Dopamine Metabolism in Rat Brain

Grol, Cor J.,Rollema, Hans,Dijkstra, Durk,Westernik, Ben H. C.

, p. 322 - 324 (1980)

The synthesis of thieno-, thieno-, and thienobenzothiazines with a hydroxyethylpiperazinylpropyl side chain and various 2 substituents is described.The influence of these neuroleptic compounds on dopamine metabolism in vivo is quantitated by determining the rise in homovanillic acid concentrations in rat corpus striatum.Notable differences in activity were found among the isomers, which were useful for structure-activity correlations in the phenothiazine neuroleptics.

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