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24370-69-2

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24370-69-2 Usage

General Description

1H-Indole-3-carboxylic acid, 5-hydroxy-, ethyl ester is a chemical compound with the molecular formula C11H11NO3. It is an ethyl ester derivative of 1H-indole-3-carboxylic acid, a naturally occurring compound found in certain plants and fungi. This chemical has been studied for its potential pharmaceutical and biological applications, including its potential as a drug candidate for the treatment of various diseases. As an ethyl ester, it may also have uses in organic synthesis and as a building block for the preparation of other chemical compounds. Overall, 1H-Indole-3-carboxylic acid, 5-hydroxy-, ethyl ester is a molecule of interest in both the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 24370-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,7 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24370-69:
(7*2)+(6*4)+(5*3)+(4*7)+(3*0)+(2*6)+(1*9)=102
102 % 10 = 2
So 24370-69-2 is a valid CAS Registry Number.

24370-69-2SDS

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 Ethyl 5-hydroxy-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 5-hydroxy-indole-3-carboxylic acid ethyl ester

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:24370-69-2 SDS

24370-69-2Downstream Products

24370-69-2Relevant articles and documents

Identification and characterization of m4 selective muscarinic antagonists

Augelli-Szafran, Corinne E.,Jaen, Juan C.,Moreland, David W.,Nelson, Carrie B.,Penvose-Yi, Jan R.,Schwarz, Roy D.

, p. 1991 - 1996 (2007/10/03)

Our interest in the area of m4 muscarinic antagonists has led us to study a series of benzoxazine isoquinolines. One of the most potent and selective compounds of this series is example 1 with an IC50 value of 90.7nM at m4 receptors, and 72-fold (m1), 38-fold (m2), 10-fold (m3), and 82- fold (m5) more selective compared to the other receptors. The synthesis and receptor binding affinity of analogs of 1 are reported.

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