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1314077-71-8

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1314077-71-8 Usage

General Description

1H-Indole-7-carboxylic acid, 4-methyl-, ethyl ester is a chemical compound with the molecular formula C13H13NO2. It is an ethyl ester derivative of 1H-indole-7-carboxylic acid, and its structure contains an indole ring with a carboxylic acid group at the 7-position and a methyl group at the 4-position. 1H-Indole-7-carboxylic acid, 4-methyl-, ethyl ester is commonly used in organic synthesis and pharmaceutical research due to its potential biological and pharmacological properties. It may have applications in the development of new drugs, as well as in the study of indole-containing natural products and their derivatives. Additionally, it may be used as a precursor in the synthesis of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1314077-71-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,0,7 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1314077-71:
(9*1)+(8*3)+(7*1)+(6*4)+(5*0)+(4*7)+(3*7)+(2*7)+(1*1)=128
128 % 10 = 8
So 1314077-71-8 is a valid CAS Registry Number.

1314077-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-methyl-1H-indole-7-carboxylate

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1314077-71-8 SDS

1314077-71-8Upstream product

1314077-71-8Downstream Products

1314077-71-8Relevant articles and documents

A new one-pot synthesis of polysubstituted indoles from pyrroles and β-nitroacrylates

Palmieri, Alessandro,Gabrielli, Serena,Lanari, Daniela,Vaccaro, Luigi,Ballini, Roberto

experimental part, p. 1425 - 1428 (2011/08/03)

The reaction of β-nitroacrylates with pyrroles, under solvent- and catalyst-free conditions, allows the formation of Friedel-Crafts adducts which, after in situ treatment with Amberlyst 15 in isopropyl alcohol under reflux, provide polysubstituted indoles, via a benzannulation reaction, in a one-pot process. Copyright

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