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4-HYDROXY-1H-INDOLE-6-CARBOXYLIC ACID METHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77140-48-8

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77140-48-8 Usage

Uses

Methyl 4-hydroxyindole-6-carboxylate is used as a pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 77140-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,4 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77140-48:
(7*7)+(6*7)+(5*1)+(4*4)+(3*0)+(2*4)+(1*8)=128
128 % 10 = 8
So 77140-48-8 is a valid CAS Registry Number.
InChI:InChI=1S/C10H9NO3/c1-14-10(13)6-4-8-7(2-3-11-8)9(12)5-6/h2-5,11-12H,1H3

77140-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-hydroxy-1H-indole-6-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 4-hydroxy-1H-indole-6-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:77140-48-8 SDS

77140-48-8Relevant academic research and scientific papers

Flexible synthesis of diverse N-heterocycles from substrates attainable from biomass

Bhusal, Ram Prasad,Sperry, Jonathan

, p. 2453 - 2459 (2016)

A suite of diverse N-heterocycles including dihydroindolone, indole, dihydroindolizinone, 2-pyridone, pyrido[1,2-a]indole, dihydrocarbazolone and carbazole have all been prepared from dimethyl itaconate and pyrrole, two compounds attainable from biomass.

A reinvestigation of 4-hydroxyindole-6-carboxylate synthesis from pyrrole-2-carboxaldehyde: A facile synthesis of indoles and indolizines

Kim, Musong,Vedejs, Edwin

, p. 6945 - 6948 (2007/10/03)

Cyclization of the Stobbe product 3 under the literature conditions (acetic anhydride/sodium acetate) affords both the indole 6 and the indolizine 8. The presence of base promotes the formation of indolizine products, and using acetic anhydride/triethylamine leads to indolizine products in good yield. Improved conditions for conversion to indoles 2, 5, and 6 are reported, and inconsistencies in some of the literature structure assignments and characterization data are noted.

Aminopropanol substituted indole compounds and compositions for the treatment of cardiac and circulatory diseases

-

, (2008/06/13)

New aminopropanol compounds of the formula STR1 wherein R is lower alkyl, cycloalkyl or alkylthioalkyl, R1 is hydrogen or lower alkyl, hydroxyalkyl, pivaloyloxyalkyl, alkoxyalkyl, alkoxycarbonyl, carboxyl or --CONR3 R4, in which R3 and R4 which can be the same or different, represent hydrogen or lower alkyl, and R2 is lower alkyl, hydroxyalkyl, alkoxyalkyl or pivaloyloxyalkyl or, when R is alkylthioalkyl or R1 is pivaloyloxyalkyl, R2 can also be hydrogen and the pharmacologically acceptable salts thereof; are outstandingly effective in the treatment or prophylaxis of cardiac and circulatory diseases.

Aminopropanol compounds and compositions for the treatment of cardiac and circulatory diseases

-

, (2008/06/13)

New aminopropanol compounds of the formula STR1 wherein R is lower alkyl, cycloalkyl or alkylthioalkyl, R1 is hydrogen or lower alkyl, hydroxyalkyl, pivaloyloxyalkyl, alkoxyalkyl, alkoxycarbonyl, carboxyl or --CONR3 R4, in which R3 and R4 which can be the same or different, represent hydrogen or lower alkyl, and R2 is lower alkyl, hydroxyalkyl, alkoxyalkyl or pivaloyloxyalkyl or, when R is alkylthioalkyl or R1 is pivaloyloxyalkyl, R2 can also be hydrogen and The pharmacologically acceptable salts thereof; are outstandingly effective in the treatment or prophylaxis of cardiac and circulatory diseases.

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