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158697-66-6

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158697-66-6 Usage

General Description

Risperidone impurity B, also known as 9-hydroxyrisperidone, is a chemical impurity that can be found in the anti-psychotic medication Risperidone. It is a metabolite of Risperidone and is formed in the body through the action of the enzyme CYP2D6. Risperidone impurity B is considered a major metabolite of Risperidone and contributes to the therapeutic effects and side effects of the medication. It is important to monitor the levels of this impurity in the body to ensure the safe and effective use of Risperidone.

Check Digit Verification of cas no

The CAS Registry Mumber 158697-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,6,9 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158697-66:
(8*1)+(7*5)+(6*8)+(5*6)+(4*9)+(3*7)+(2*6)+(1*6)=196
196 % 10 = 6
So 158697-66-6 is a valid CAS Registry Number.

158697-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-(4-((2,4-difluorophenyl)(hydroxyimino)methyl)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names -

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:158697-66-6 SDS

158697-66-6Downstream Products

158697-66-6Relevant articles and documents

Process for making risperidone and intermediates therefor

-

Page/Page column 5, (2008/06/13)

The formation of risperidone is enhanced by the use of enriched Z-isomer oxime intermediate(s) of formula (3) or (7). The oxime(s) can be isomerically enriched by a variety of techniques including the use of the novel acetic acid salt thereof, which affords, inter alia, resolution of the isomers and/or by heat conversion.

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