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Methyl 1-(4-fluorophenyl)-1H-indole-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

206767-65-9

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206767-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206767-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,7,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 206767-65:
(8*2)+(7*0)+(6*6)+(5*7)+(4*6)+(3*7)+(2*6)+(1*5)=149
149 % 10 = 9
So 206767-65-9 is a valid CAS Registry Number.

206767-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-(4-fluorophenyl)indole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 1-(4-fluorophenyl)-1H-indole-4-carboxylate

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:206767-65-9 SDS

206767-65-9Relevant academic research and scientific papers

5-HT3 RECEPTOR MODULATORS, METHODS OF MAKING, AND USE THEREOF

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Page/Page column 35, (2009/12/23)

Novel 5-HT3 receptor modulators are disclosed. These compounds are used in the treatment of various disorders, including chemotherapy-induced nausea and vomiting, post-operative nausea and vomiting, and irritable bowel syndrome. Methods of maki

Azepinoindole derivatives with high affinity for brain dopamine and serotonin receptors

Maryanoff, Bruce E.,McComsey, David F.,Martin, Gregory E.,Shank, Richard P.

, p. 983 - 988 (2007/10/03)

We synthesized 20 and 21 as conformationally constrained analogues of the dopamine receptor antagonist SKF-83742, as well as analogues 6-9, 16, and 18-22. Although 20 and 21 were inactive, 7, 9, and 19 showed strong binding to D-1, D-2, S-2, and α-1 receptors, as well as antipsychotic activity in vivo.

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