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71526-84-6

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71526-84-6 Usage

General Description

4-chloro-2',5'-dimethylbutyrophenone, also known as clopenthixol, is a chemical compound belonging to the class of butyrophenone antipsychotic drugs. It is primarily used for the treatment of psychotic disorders such as schizophrenia, as well as for agitation and aggression in patients with behavioral disturbances. Clopenthixol works by blocking the effects of dopamine in the brain, which helps to alleviate the symptoms of psychosis and stabilize the patient’s mood. It is available in various formulations including oral tablets and injectable solutions, and should be used under the guidance of a healthcare professional due to its potential for side effects and interactions with other medications.

Check Digit Verification of cas no

The CAS Registry Mumber 71526-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,2 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71526-84:
(7*7)+(6*1)+(5*5)+(4*2)+(3*6)+(2*8)+(1*4)=126
126 % 10 = 6
So 71526-84-6 is a valid CAS Registry Number.

71526-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-1-(2,5-dimethylphenyl)butan-1-one

1.2 Other means of identification

Product number -
Other names 2',5'-dimethyl-4-chlorobutyrophenone

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:71526-84-6 SDS

71526-84-6Relevant articles and documents

A combined computational and experimental investigation of the oxidative ring-opening of cyclic ethers by oxoammonium cations

Loman, Jacob. J.,Carnaghan, Emma R.,Hamlin, Trevor A.,Ovian, John M.,Kelly, Christopher B.,Mercadante, Michael A.,Leadbeater, Nicholas E.

, p. 3883 - 3888 (2016/05/24)

The propensity of oxoammonium cations to facilitate the oxidative ring-opening of cyclic ethers to their corresponding distal hydroxy ketones is investigated. The reaction has been evaluated using experimental and computational methods to gain deeper insight into trends in reactivity.

Synthesis of some compounds derived from chlorobutyrophenones

Schliemann,Buege,Reppel

, p. 140 - 143 (2007/10/02)

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