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63176-44-3

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63176-44-3 Usage

General Description

2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID is a chemical compound with the molecular formula C10H9NO2. It is classified as an indole derivative, which is a group of organic compounds that contain a bicyclic ring structure. This specific compound is a carboxylic acid derivative of indole, with a methyl group attached to the indole ring at the 2-position. It is commonly used in the synthesis of pharmaceuticals and agrochemicals. Additionally, it has shown potential in the development of new drugs and has been studied for its biological activities, including anti-inflammatory and anticancer properties. Overall, 2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID is an important chemical in the field of medicinal and pharmaceutical chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 63176-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,7 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63176-44:
(7*6)+(6*3)+(5*1)+(4*7)+(3*6)+(2*4)+(1*4)=123
123 % 10 = 3
So 63176-44-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c1-6-9(10(12)13)7-4-2-3-5-8(7)11-6/h2-5,11H,1H3,(H,12,13)

63176-44-3SDS

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 2-Methyl-1H-indole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID

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:63176-44-3 SDS

63176-44-3Relevant articles and documents

Transformations of phenylhydrazones of dialkyl 2-oxo-propane-1,3- dicarboxylate and of ethyl acetoacetate in concentrated sulfuric acid

Bevk, David,Svete, Jurij,Stanovnik, Branko

, p. 1413 - 1415 (2007/10/03)

The hydrazones 3a,b, prepared from phenylhydrazine (1) and dialkyl 2-oxopropane-1,3-dicarboxylate (2a,b) were converted in concentrated sulfuric acid at -5 °C into a mixture of alkyl (3-carboxyindol-2-yl)acetates (5a,b), and ethyl (5-ethoxy-1-phenyl-1H-pyrazol-3-yl)acetate 6. The hydrazone 8, prepared from 1 and ethyl acetoacetate (7) was transformed under the same conditions into a mixture of five compounds: ethyl 2-methylindol-3-carboxylate (9), 2-methylindol-3-carboxylic acid (10), 2-methylindol (11), 5-ethoxy-3-methyl-1-phenyl-1H-pyrazole (12), and 3-methyl-1-phenyl-1H-pyrazol-5- one (13).

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