10408-52-3 Usage
Description
(4-ethylphenyl)(hydroxy)acetic acid, also known as ethyl (hydroxy)phenylacetic acid, is a derivative of phenylacetic acid. It is an aromatic carboxylic acid that consists of a hydroxy group, an ethyl group, and a phenyl group attached to a carboxylic acid functional group. (4-ethylphenyl)(hydroxy)acetic acid is commonly used in the production of various pharmaceuticals and drugs due to its anti-inflammatory and analgesic properties.
Uses
Used in Pharmaceutical Industry:
(4-ethylphenyl)(hydroxy)acetic acid is used as an active pharmaceutical ingredient for the development of drugs with anti-inflammatory and analgesic properties. Its ability to reduce inflammation and alleviate pain makes it useful in the treatment of various conditions.
Used as an Intermediate in Organic Synthesis:
(4-ethylphenyl)(hydroxy)acetic acid is used as an important intermediate in the synthesis of other organic compounds. Its unique structure and properties allow it to be a key component in the production of various chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 10408-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,0 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10408-52:
(7*1)+(6*0)+(5*4)+(4*0)+(3*8)+(2*5)+(1*2)=63
63 % 10 = 3
So 10408-52-3 is a valid CAS Registry Number.
10408-52-3Relevant articles and documents
Substituted amide phenol compound and its preparation method, pharmaceutical composition and use thereof
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Paragraph 0294-0297, (2019/07/04)
The invention discloses substituted-amide phenolic compounds, their preparation method, a pharmaceutical composition and an application thereof. The compounds have a structure as shown in the general formula I, wherein Z, L and Q are as defined in the spe
N-(1-ARYL-2,2,2-TRIHALOGENOETHYL)CARBOXAMIDES
Bal'on, Ya. G.,Smirnov, V. A.
, p. 2051 - 2054 (2007/10/02)
The readily obtained products from the condensation of trihalogenoacetaldehydes with carboxamides react with benzene and its homologs in the presence of concentrated sulfuric acid with the formation of N-(1-aryl-2,2,2-trihalogenoethyl)carboxamides.The latter were used for the production of 1-aryl-2,2,2-trihalogenoethylamines and 1-acylimino-1-aryl-2,2,2-trihalogenoethanes.