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73967-75-6

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73967-75-6 Usage

Chemical Class

1H-Indole-3-carboxylic acid derivatives

Explanation

The compound belongs to a class of chemical compounds derived from 1H-indole-3-carboxylic acid.

Explanation

The compound is a methyl ester derivative, which means it has an ester functional group (-COO-) attached to a methyl group (-CH3).

Explanation

A hydroxyl group is present at the 5th position of the indole ring, which may contribute to its biological activity and ligand-receptor interactions.

Explanation

A methyl group is attached to the 2nd position of the indole ring, which can influence the compound's pharmacological properties.

Explanation

The compound has a phenylmethyl substituent, which is a phenyl group (-C6H5) attached to a methylene group (-CH2-). This structural feature contributes to its similarity to serotonin and other biologically active indole compounds.

Explanation

The compound's structural similarity to serotonin and other biologically active indole compounds suggests that it may have potential as a pharmacological agent.

Explanation

The presence of a hydroxyl group and a phenylmethyl substituent may contribute to the compound's biological activity, as these groups are often involved in ligand-receptor interactions and enzymatic reactions.

Explanation

More research is needed to fully understand the potential pharmacological effects and applications of this compound.

Methyl Ester

Methyl ester functional group

Hydroxyl Group

Presence of a hydroxyl group (-OH) at the 5th position

Methyl Group

Methyl group (-CH3) at the 2nd position

Phenylmethyl Substituent

Presence of a phenylmethyl group (-CH2-C6H5)

Potential Pharmacological Properties

Possible activity as a pharmacological agent

Biological Activity

Potential for biological activity due to hydroxyl and phenylmethyl groups

Further Research

Exploration of potential pharmacological effects and applications

Check Digit Verification of cas no

The CAS Registry Mumber 73967-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73967-75:
(7*7)+(6*3)+(5*9)+(4*6)+(3*7)+(2*7)+(1*5)=176
176 % 10 = 6
So 73967-75-6 is a valid CAS Registry Number.

73967-75-6SDS

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 3-(carbomethoxy)-2-methyl-1-(phenylmethyl)-5-hydroxyindole

1.2 Other means of identification

Product number -
Other names 1-Benzyl-5-hydroxy-2-methylindol-3-carbonsaeuremethylester

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:73967-75-6 SDS

73967-75-6Relevant articles and documents

Synthesis of indomethacin analogues for evaluation as modulators of MRP activity

Maguire, Anita R.,Plunkett, Stephen J.,Papot, Sébastien,Clynes, Martin,O'Connor, Robert,Touhey, Samantha

, p. 745 - 762 (2007/10/03)

Synthesis of a range of indomethacin analogues, required for investigation in combination toxicity assays, bearing both N-benzyl and N-benzoyl groups, is described. Copyright

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