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5165-45-7

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5165-45-7 Usage

Chemical class

Indole derivatives

Structure

1H-Indole-3-carboxylic acid, 5-hydroxy-2-methyl-1-(4-methylphenyl)-, ethyl ester

Type

Ethyl ester derivative

Biological activities

Antioxidant and anti-inflammatory properties

Therapeutic potential

Potential therapeutic agent for various diseases, including cancer and neurological disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 5165-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,6 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5165-45:
(6*5)+(5*1)+(4*6)+(3*5)+(2*4)+(1*5)=87
87 % 10 = 7
So 5165-45-7 is a valid CAS Registry Number.

5165-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Hydroxy-2-methyl-1-p-tolyl-1H-indole-3-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names -

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:5165-45-7 SDS

5165-45-7Relevant articles and documents

α-d-Galacturonic Acid as Natural Ligand for Selective Copper-Catalyzed N-Arylation of N-Containing Heterocycles

Yuan, Chunling,Zhao, Yingdai,Zheng, Li

, p. 2173 - 2180 (2019/11/25)

The first application of α-d-galacturonic acid hydrate (GalA) is reported here, as a potential O-donor ligand. The C-N couplings of N-heterocycles with aryl halides or arylboronic acids could be readily conducted and exhibited good functional group tolerance with characters of selectivity. These N-Arylazoles allow rapid access to several pharmaceutical intermediates and can be easily transformed into a variety of other interesting scaffolds as well.

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