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185212-25-3

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185212-25-3 Usage

Structure

An ester derivative of indole-2-carboxylic acid with a 4-ethoxy substitution on the phenyl ring and a methyl ester functional group

Occurrence

Commonly found in various plant and animal tissues

Uses

In the synthesis of pharmaceuticals and agrochemicals

Pharmacological activities

Potential antifungal, antibacterial, and anti-inflammatory properties

Stability and bioavailability

Improved by the methyl ester functional group, making it a valuable building block for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 185212-25-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,2,1 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 185212-25:
(8*1)+(7*8)+(6*5)+(5*2)+(4*1)+(3*2)+(2*2)+(1*5)=123
123 % 10 = 3
So 185212-25-3 is a valid CAS Registry Number.

185212-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-ethoxyindole-2-carboxylate

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:185212-25-3 SDS

185212-25-3Upstream product

185212-25-3Downstream Products

185212-25-3Relevant articles and documents

Tripeptidylpeptidase inhibitors

-

, (2008/06/13)

A compound of formula wherein the substituents are defined as in the specification and salts or hydrates thereof is disclosed as well as a method of treating disorders associated with the inactivation or excessive degradation of cholecystokinin.

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