625095-56-9 Usage
Description
(S)-(-)-(3-chlorophenyl)-3-hydroxypropionic acid, also known as mandelic acid, is a chiral compound with the chemical formula C8H8O3Cl. It is a white crystalline solid that is soluble in water and ethanol. As a naturally occurring form, it possesses unique properties that make it valuable in various applications.
Used in Pharmaceutical Industry:
(S)-(-)-(3-chlorophenyl)-3-hydroxypropionic acid is used as a precursor in the synthesis of pharmaceuticals for its ability to be chemically modified and incorporated into various drug molecules, contributing to the development of new medications.
Used in Chemical Production:
(S)-(-)-(3-chlorophenyl)-3-hydroxypropionic acid is used as a starting material in the production of various chemicals, leveraging its unique structure to create a range of different compounds for industrial use.
Used in Cosmetics Industry:
(S)-(-)-(3-chlorophenyl)-3-hydroxypropionic acid is used as an active ingredient in cosmetic products due to its antibacterial and anti-inflammatory properties, making it suitable for skincare treatments targeting acne and hyperpigmentation.
Used in Urinary Tract Infection Treatment:
(S)-(-)-(3-chlorophenyl)-3-hydroxypropionic acid is being investigated for its potential use in treating urinary tract infections, suggesting that it may have therapeutic benefits in combating such conditions.
As a chiral compound, (S)-(-)-(3-chlorophenyl)-3-hydroxypropionic acid's distinct properties in comparison to its enantiomer, (R)-(+)-mandelic acid, make it a versatile and valuable substance across different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 625095-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,5,0,9 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 625095-56:
(8*6)+(7*2)+(6*5)+(5*0)+(4*9)+(3*5)+(2*5)+(1*6)=159
159 % 10 = 9
So 625095-56-9 is a valid CAS Registry Number.
625095-56-9Relevant articles and documents
NOVEL 2'-C-METHYL AND 4'-C-METHYL NUCLEOSIDE DERIVATIVES
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Page/Page column 111-113, (2008/06/13)
Novel 2'-C-methyl nucleoside 5 '-monophosphate and 4'-C-methyl nucleoside 5'- monophosphate derivatives, stereoisomers, and pharmaceutically acceptable salts or prodrugs thereof, their preparation, and their uses for the treatment of hepatitis C viral inf
LEWIS ACID MEDIATED SYNTHESIS OF CYCLIC ESTERS
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Page/Page column 27;28, (2008/06/13)
Methods for the synthesis of cyclic phosphonic acid diesters from 1,3-diols are described, whereby cyclic phosphonic acid diesters are produced by reacting a chiral 1,3-diol and an activated phosphonic acid in the presence of a Lewis acid.
Process for preparation of cyclic prodrugs of PMEA and PMPA
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Page 9-10, (2010/11/30)
The method of preparing compounds of Formula I is described: wherein: M and V are cis to one another and MPO3H2 is a phosphonic acid selected from the group consisting of 9-(2-phosphonylmethoxyethyl)adenine, and (R)-9-(2-phosphonylmethoxypropyl)adenine; wherein V is phenyl, optionally substituted with 1-2 substituents selected from a group consisting of fluoro, chloro, and bromo; comprising: coupling a chiral 1-phenylpropane-1,3-diol, wherein the phenyl may be optionally substituted, with MPOCl2 or an N-6 substituted analogue thereof. Additionally, methods and salt forms are described that enable isolation and purification of the desired isomer.
