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1261449-78-8

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1261449-78-8 Usage

Description

3-(2-Chloro-4-hydroxyphenyl)propionic acid, also known as CHPPA, is a chemical compound that belongs to the class of hydroxyphenylpropionic acids. It is a derivative of phenylpropanoic acid, featuring a propionic acid substituent attached to a phenyl ring that is chlorinated at the 2 position and hydroxylated at the 4 position. CHPPA has been studied for its potential pharmaceutical and therapeutic applications, including its anti-inflammatory and antioxidant properties.

Uses

Used in Pharmaceutical Industry:
3-(2-Chloro-4-hydroxyphenyl)propionic acid is used as a precursor in the synthesis of other pharmaceutical compounds for its versatile chemical structure and potential therapeutic properties.
Used in Research:
CHPPA is used as a research tool in biological and chemical studies to explore its anti-inflammatory and antioxidant properties, as well as its potential role in treating various diseases and conditions.
Used in Disease Treatment:
3-(2-Chloro-4-hydroxyphenyl)propionic acid is being investigated for its potential role in the treatment of various diseases and conditions, such as cancer and cardiovascular disorders, due to its promising pharmaceutical and therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1261449-78-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,4,4 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1261449-78:
(9*1)+(8*2)+(7*6)+(6*1)+(5*4)+(4*4)+(3*9)+(2*7)+(1*8)=158
158 % 10 = 8
So 1261449-78-8 is a valid CAS Registry Number.

1261449-78-8Upstream product

1261449-78-8Downstream Products

1261449-78-8Relevant articles and documents

GUANIDINOBENZOIC ACID COMPOUND

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Paragraph 0155; 0222, (2014/08/06)

[Problem] Provided is a compound which is useful as an agent for preventing and/or treating renal diseases. [Means for Solution] The present inventors have conducted extensive studies on compounds having a trypsin inhibitory action, and as a result, they

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