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1-(hydroxymethyl)-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid is a complex chemical compound featuring a four-ring tetrahydro-beta-carboline core, with a carboxylic acid group and a hydroxymethyl group attached to it. Although not extensively studied, its structural similarity to psychoactive and medicinal beta-carbolines suggests potential biological activity. The carboxylic acid group also makes it a promising building block for synthesizing other compounds, and its unique structure may be valuable for pharmaceutical or scientific research.

73198-02-4

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73198-02-4 Usage

Uses

Used in Pharmaceutical Industry:
1-(hydroxymethyl)-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid is used as a potential building block for the synthesis of other compounds due to its carboxylic acid group, which can facilitate the creation of new pharmaceutical agents.
Used in Scientific Research:
1-(hydroxymethyl)-2,3,4,9-tetrahydro-1H-beta-carboline-3-carboxylic acid is used as a subject of study in scientific research to explore its biological activity and potential applications, given its structural similarity to known psychoactive and medicinal beta-carbolines.

Check Digit Verification of cas no

The CAS Registry Mumber 73198-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,9 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73198-02:
(7*7)+(6*3)+(5*1)+(4*9)+(3*8)+(2*0)+(1*2)=134
134 % 10 = 4
So 73198-02-4 is a valid CAS Registry Number.

73198-02-4SDS

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 1-(hydroxymethyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names optically inactive 1.3-diacetoxy-cyclohexane

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:73198-02-4 SDS

73198-02-4Relevant 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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