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39537-10-5

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39537-10-5 Usage

Description

(S)-4,9-DIHYDRO-1-METHYL-3H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID is a complex chemical compound that belongs to the carboxylic acid class, characterized by the presence of a carboxyl group (-COOH) in its molecular structure. (S)-4,9-DIHYDRO-1-METHYL-3H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID features a pyridoindole core, with a methyl group and a carboxylic acid functional group attached to distinct positions within the core. Due to its structural resemblance to other bioactive compounds, it may hold promise in the fields of medicinal chemistry and drug development. However, further research is required to ascertain its specific properties and potential applications.

Uses

Used in Pharmaceutical Industry:
(S)-4,9-DIHYDRO-1-METHYL-3H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID is used as a potential candidate in drug development for its structural similarity to known bioactive compounds, which may indicate pharmacological activity. (S)-4,9-DIHYDRO-1-METHYL-3H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID's unique molecular structure, including the pyridoindole core and functional groups, could be harnessed to create novel therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (S)-4,9-DIHYDRO-1-METHYL-3H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID serves as a subject of study to understand its interactions with biological targets and its potential to modulate various biological pathways. This research could lead to the discovery of new drugs or drug candidates with specific therapeutic effects.
Please note that the provided materials do not specify any direct applications for (S)-4,9-DIHYDRO-1-METHYL-3H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID. The uses listed above are inferred based on the compound's classification and structural characteristics, suggesting potential areas of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 39537-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,3 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39537-10:
(7*3)+(6*9)+(5*5)+(4*3)+(3*7)+(2*1)+(1*0)=135
135 % 10 = 5
So 39537-10-5 is a valid CAS Registry Number.

39537-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-1-methyl-3,4-dihydro-2H-pyrido[3,4-b]indole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3H-Pyrido[3,4-b]indole-3-carboxylicacid,4,9-dihydro-1-methyl-,(S)-(9CI)

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:39537-10-5 SDS

39537-10-5Relevant articles and documents

Electrochemistry of Natural Products. 7. Oxidative Decarboxylation of Some Tetrahydro-β-carbolinecarboxylic Acids

Bobbitt, James M.,Willis, John P.

, p. 1978 - 1984 (2007/10/02)

A series of 1,2,3,4-tetrahydro-β-carboline-1- and -3-carboxylic acids containing various substituents in positions 1, 2, and 3 were oxidized electrochemically.In general, the acids were decarboxylated, and unsaturation was introduced into the C ring.The oxidation appears to take place through the indole ring nitrogen, and possible mechanisms of the reactions are presented.Parallels between the observed reactions and early steps in indole alkaloid biosynthesis are discussed.The oxidative dimerization of tetrahydrocarbazole is reported.

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