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4-chloro-N-(3-methyl-1-phenyl-indol-2-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138349-55-0

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138349-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138349-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,4 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138349-55:
(8*1)+(7*3)+(6*8)+(5*3)+(4*4)+(3*9)+(2*5)+(1*5)=150
150 % 10 = 0
So 138349-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H17ClN2O/c1-15-19-9-5-6-10-20(19)25(18-7-3-2-4-8-18)21(15)24-22(26)16-11-13-17(23)14-12-16/h2-14H,1H3,(H,24,26)

138349-55-0SDS

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 4-chloro-N-(3-methyl-1-phenylindol-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names 4-CHLORO-N-(3-METHYL-1-PHENYL-INDOL-2-YL)BENZAMIDE

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:138349-55-0 SDS

138349-55-0Downstream Products

138349-55-0Relevant articles and documents

Visible light C-H amidation of heteroarenes with benzoyl azides

Brachet,Ghosh,Ghosh,K?nig

supporting information, p. 987 - 992 (2015/02/19)

Benzoyl azides were used for the direct and atom economic C-H amidation of electron rich heteroarenes in the presence of phosphoric acid, a photocatalyst and visible light. Hetero-aromatic amides are obtained in good yields at very mild reaction conditions with dinitrogen as the only by-product. The reaction allows the use of aryl-, heteroaryl- or alkenyl acyl azides and has a wide scope for heteroarenes, including pyrroles, indole, furan, benzofuran and thiophene giving good regio-selectivities and yields.

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