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1008531-60-9

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1008531-60-9 Usage

Chemical Properties

Off-White to Tan Powder

Uses

Different sources of media describe the Uses of 1008531-60-9 differently. You can refer to the following data:
1. A metabolite of Aripiprazole, a selective dopamine D2-receptor antagonist with dopamine autoreceptor agonist activity
2. Dehydro Aripiprazole Hydrochloride is a metabolite of Aripiprazole, a selective dopamine D2-receptor antagonist with dopamine autoreceptor agonist activity.

Check Digit Verification of cas no

The CAS Registry Mumber 1008531-60-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,8,5,3 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1008531-60:
(9*1)+(8*0)+(7*0)+(6*8)+(5*5)+(4*3)+(3*1)+(2*6)+(1*0)=109
109 % 10 = 9
So 1008531-60-9 is a valid CAS Registry Number.

1008531-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-[4-[4-(2,3-dichlorophenyl)piperazin-1-yl]butoxy]-1H-quinolin-2-one,hydrochloride

1.2 Other means of identification

Product number -
Other names Dehydro Aripiprazole Hydrochloride

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:1008531-60-9 SDS

1008531-60-9Upstream product

1008531-60-9Downstream Products

1008531-60-9Relevant articles and documents

Preparation method and application of substituted quinoline-2(1H)-one compound

-

Paragraph 0081-0084, (2019/11/29)

The invention belongs to the field of pharmaceutical chemistry and chemical synthesis, and concretely relates to a preparation method of a substituted quinoline-2(1H)-one compound. The invention provides a preparation method of the substituted quinoline-2(1H)-one compound. The preparation method performs an oxidation reaction on a compound represented by a formula I and an oxidant in a solvent toobtain a compound represented by a formula II. The preparation method has the advantages of simple method, high yield and low cost and is suitable for industrial production. The substituted quinoline-2(1H)-one represented by the formula II is an important intermediate of a variety of pharmaceutical active ingredients.

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