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138900-22-8

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138900-22-8 Usage

Chemical Properties

Light Yellow to Light Orange Solid

Uses

5-Chloro-1-(4-fluorophenyl)indole can be used in the preparation of serotoninergic S2 antagonists.

Check Digit Verification of cas no

The CAS Registry Mumber 138900-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,0 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138900-22:
(8*1)+(7*3)+(6*8)+(5*9)+(4*0)+(3*0)+(2*2)+(1*2)=128
128 % 10 = 8
So 138900-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H9ClFN/c15-11-1-6-14-10(9-11)7-8-17(14)13-4-2-12(16)3-5-13/h1-9H

138900-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-1-(4-fluorophenyl)-1H-indole

1.2 Other means of identification

Product number -
Other names 5-chloro-1-(4-fluorophenyl)indole

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:138900-22-8 SDS

138900-22-8Relevant articles and documents

Identification and synthesis of impurities formed during sertindole preparation

Sunil Kumar,Anjaneyulu,Hima Bindu

supporting information; scheme or table, p. 29 - 33 (2011/03/22)

Sertindole (1), an atypical anti-psychotic drug is used for the treatment of schizophrenia. During the laboratory optimization and later during its bulk synthesis the formation of various impurities was observed. The impurities formed were monitored and t

Process for the preparation of 5-chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)indole and method of manufacturing sertindole

-

Example 4, (2010/01/31)

A process of manufacturing sertindole comprising reacting 5-chloro-1-(4-fluorophenyl)indole with 4-piperidone in a mixture of an acetic acid and concentrated HCl; reduction of the resulting 5-chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)indole and reaction of this compound with 1-(2-chloroethyl)-2-imidazolidinon in order to obtain sertindole.

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