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10078-25-8

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10078-25-8 Usage

Uses

Perphenazine Sulfoxide (Perphenazine EP Impurity A) acts as a D2 dopamine receptor antagonist; α-adrenergic receptor antagonist and σ-receptor agonist; phenothiazine antipsychotic. Inhibits glutamate dehydrogenase in vitro. Antipsychotic.

Check Digit Verification of cas no

The CAS Registry Mumber 10078-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,7 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10078-25:
(7*1)+(6*0)+(5*0)+(4*7)+(3*8)+(2*2)+(1*5)=68
68 % 10 = 8
So 10078-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H26ClN3O2S/c22-17-6-7-21-19(16-17)25(18-4-1-2-5-20(18)28(21)27)9-3-8-23-10-12-24(13-11-23)14-15-26/h1-2,4-7,16,26H,3,8-15H2

10078-25-8 Well-known Company Product Price

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  • (1511203)  Perphenazine sulfoxide  United States Pharmacopeia (USP) Reference Standard

  • 10078-25-8

  • 1511203-100MG

  • 14,578.20CNY

  • Detail

10078-25-8SDS

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 PERPHENAZINE SULFOXIDE (100 MG)

1.2 Other means of identification

Product number -
Other names 4-(3-(2-chlorophenothiazin-10-yl)propyl)-1-piperazineethanosulfoxide

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10078-25-8 SDS

10078-25-8Upstream product

10078-25-8Downstream Products

10078-25-8Relevant articles and documents

Convenient oxidation of phenothiazine salts to their sulfoxides with aqueous nitrous acid

Owens,Juenge,Poklis

, p. 334 - 336 (1989)

A simple method is reported for the preparation of gram quantities of phenothiazine sulfoxides by aqueous nitrous acid oxidation of phenothiazines at room temperature. The chiral levomepromazine gave rise to diastereoisomeric products analogous to those reported for thioridazine sulfoxidation.

Studies on phenothiazines. 2. Synthesis of a 10 N--substituted phenothiazine sulfoxide and its spectroscopic characterization

Kreyenbuehl,Joshi,Perlia

, p. 248 - 252 (2007/10/04)

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