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1H-Indole-3-carboxylic acid, 6-hydroxy-, methyl ester is a chemical compound belonging to the indole class of organic compounds. It is characterized by its potential therapeutic applications, including anti-inflammatory, anti-cancer, and anti-microbial properties. The methyl ester form enhances its solubility and bioavailability, making it a suitable candidate for medicinal formulations. This versatile and important chemical plays a significant role in the development of pharmaceutical products and offers potential therapeutic benefits.

112332-97-5

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112332-97-5 Usage

Uses

Used in Pharmaceutical Industry:
1H-Indole-3-carboxylic acid, 6-hydroxy-, methyl ester is used as a precursor in the synthesis of various drugs and pharmaceutical products. Its versatile chemical properties and potential therapeutic benefits make it an important component in the development of new medications.
Used in Anti-inflammatory Applications:
1H-Indole-3-carboxylic acid, 6-hydroxy-, methyl ester is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate associated symptoms. Its anti-inflammatory properties can be beneficial in treating various inflammatory conditions.
Used in Anti-cancer Applications:
1H-Indole-3-carboxylic acid, 6-hydroxy-, methyl ester is used as an anti-cancer agent for its potential to inhibit the growth and proliferation of cancer cells. Its anti-cancer properties can be utilized in the development of new therapeutic strategies for cancer treatment.
Used in Anti-microbial Applications:
1H-Indole-3-carboxylic acid, 6-hydroxy-, methyl ester is used as an anti-microbial agent for its potential to inhibit the growth of microorganisms, including bacteria and fungi. Its anti-microbial properties can be employed in the development of new antimicrobial drugs and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 112332-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112332-97:
(8*1)+(7*1)+(6*2)+(5*3)+(4*3)+(3*2)+(2*9)+(1*7)=85
85 % 10 = 5
So 112332-97-5 is a valid CAS Registry Number.

112332-97-5SDS

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 6-hydroxy-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 6-Hydroxyhex-2-insaeuremethylester

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:112332-97-5 SDS

112332-97-5Relevant articles and documents

BICYCLIC AMIDES AS KINASE INHIBITORS

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Page/Page column 74, (2010/11/08)

The invention relates to compounds of formula (I) and their use in the treatment of the animal or human body, to pharmaceutical compositions comprising a compound of formula I and to the use of a compound of formula I for the preparation of pharmaceutical compositions for use in the treatment of protein kinase dependent diseases, especially of proliferative diseases, such as in particular tumour diseases.

Synthesis and pharmacological activity of metabolites of the 5-HT4 receptor antagonist SB-207266

Fedouloff, Michael,Hossner, Frank,Voyle, Martyn,Ranson, Jennie,Powles, Jenifer,Riley, Graham,Sanger, Gareth

, p. 2119 - 2128 (2007/10/03)

Three metabolites of N-[(1-butyl-4-piperidinyl)methyl]-3,4-dihydro-2H-[1,3]-oxazino[3,2_a]indole- 10-carboxamide (SB-207266) (1) were synthesised and their pharmacological activity determined.

INTRODUCTION OF A HYDROXY GROUP ONTO 5- AND 6-POSITION OF INDOLE NUCLEUS BY FRIEDEL-CRAFTS ACYLATION AND SUBSEQUENT BAYER-VILLIGER OXIDATION

Nakatsuka, Shin-ichi,Asano, Osamu,Ueda, Kazuo,Goto, Toshio

, p. 1471 - 1474 (2007/10/02)

A hydroxy group was efficiently introduced onto 5- and 6-position of methyl 1-methylindole-3-carboxylate 1 and methyl indole-3-carboxylate 11.

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