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2,3,4,9-Tetrahydro-1H-pyrido(3,4-b)indole-1,3-dicarboxylic acid is a complex heterocyclic compound characterized by a pyridine ring fused to an indole ring and the presence of two carboxylic acid groups. It is not commonly found in nature but can be synthesized in the laboratory. Its potential uses are not well-documented, but its structure suggests that it may have applications in medicinal chemistry, such as for drug development or as a molecular probe in biological research.

59132-30-8

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59132-30-8 Usage

Uses

Used in Medicinal Chemistry:
2,3,4,9-Tetrahydro-1H-pyrido(3,4-b)indole-1,3-dicarboxylic acid is used as a potential candidate for drug development due to its unique structure and the presence of carboxylic acid groups that can facilitate interactions with biological targets.
Used in Biological Research:
2,3,4,9-Tetrahydro-1H-pyrido(3,4-b)indole-1,3-dicarboxylic acid is used as a molecular probe in biological research to investigate its interactions with various biological systems and to explore its potential as a tool for studying related compounds and mechanisms.
Further studies are needed to fully understand the properties and potential uses of this chemical compound in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 59132-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,3 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59132-30:
(7*5)+(6*9)+(5*1)+(4*3)+(3*2)+(2*3)+(1*0)=118
118 % 10 = 8
So 59132-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O4/c16-12(17)9-5-7-6-3-1-2-4-8(6)14-10(7)11(15-9)13(18)19/h1-4,9,11,14-15H,5H2,(H,16,17)(H,18,19)

59132-30-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-1,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 1H-Pyrido(3,4-b)indole-1,3-dicarboxylic acid,2,3,4,9-tetrahydro

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:59132-30-8 SDS

59132-30-8Downstream Products

59132-30-8Relevant academic research and scientific papers

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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