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1-ACETYL-6-METHOXYCARBONYLINDOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126759-62-4

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126759-62-4 Usage

Chemical structure

A derivative of indole with an acetyl group and a methoxycarbonyl group attached to the 1 and 6 positions, respectively.

Type of compound

Synthetic intermediate

Usage

Used in research and pharmaceutical development

Applications

Potential applications in the synthesis of various organic compounds and pharmaceuticals

Interest to scientists

Studied for its properties and reactivity as an indole derivative

Pharmacological activities

Investigated for potential pharmacological activities

Information source

Specific information regarding its uses and effects must be obtained from reliable and authoritative sources.

Check Digit Verification of cas no

The CAS Registry Mumber 126759-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,5 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126759-62:
(8*1)+(7*2)+(6*6)+(5*7)+(4*5)+(3*9)+(2*6)+(1*2)=154
154 % 10 = 4
So 126759-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO3/c1-8(14)13-6-5-9-3-4-10(7-11(9)13)12(15)16-2/h3-7H,1-2H3

126759-62-4SDS

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 methyl 1-acetylindole-6-carboxylate

1.2 Other means of identification

Product number -
Other names 6-methoxycarbonyl-N-acetylindole

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:126759-62-4 SDS

126759-62-4Relevant academic research and scientific papers

Rhodium-Catalyzed β-Selective Oxidative Heck-Type Coupling of Vinyl Acetate via C-H Activation

Zhang, Hui-Jun,Lin, Weidong,Su, Feng,Wen, Ting-Bin

supporting information, p. 6356 - 6359 (2016/12/23)

An efficient Rh(III)-catalyzed direct ortho-C-H olefination of acetanilides with vinyl acetate was developed. This protocol provides a straightforward pathway to a series of (E)-2-acetamidostyryl acetates, giving access to indole derivatives following a simple hydrolysis/cyclization process.

A Regiocontrolled Synthesis of Substituted Indoles by Palladium-Catalyzed Coupling of 2-Bromonitrobenzenes and 2-Bromoacetanilides

Kasahara, Akira,Izumi, Taeko,Murakami, Satoshi,Miyamoto, Kazuhiro,Hino, Toshimi

, p. 1405 - 1413 (2007/10/02)

The palladium-catalyzed cross-coupling reaction of 2-bromonitrobenzenes or 2-bromoacetanilides with ethylene has been used to produce a variety of substituted indoles.The mild reaction conditions and selectivity inherent in the coupling reaction have been utilized to produce regiochemically pure 4-, 5-, 6-, and 7-substituted indoles.

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