13057-65-3 Usage
Description
Beta-(2-methoxyphenoxy)lactic acid, also known as 3-(2-methoxyphenoxy)lactic acid, is a metabolite derived from Guaifenesin (G810500), which is a centrally acting muscle relaxant with expectorant properties. beta-(2-methoxyphenoxy)lactic acid is characterized by its unique chemical structure that features a methoxyphenoxy group attached to a lactic acid backbone.
Uses
Used in Pharmaceutical Industry:
Beta-(2-methoxyphenoxy)lactic acid is used as an intermediate compound for the synthesis of various pharmaceutical products. Its role in the metabolism of Guaifenesin, a muscle relaxant and expectorant, makes it a valuable component in the development of medications targeting muscle relaxation and respiratory health.
Used in Metabolic Research:
As a metabolite of Guaifenesin, beta-(2-methoxyphenoxy)lactic acid is utilized in metabolic research to study the biotransformation processes of the parent compound. This research can provide insights into the metabolic pathways and potential therapeutic applications of Guaifenesin and its derivatives.
Used in Drug Development:
The unique chemical structure of beta-(2-methoxyphenoxy)lactic acid makes it a potential candidate for the development of new drugs with muscle relaxant and expectorant properties. Researchers can explore its potential in creating novel therapeutic agents that may offer improved efficacy and reduced side effects compared to existing treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 13057-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13057-65:
(7*1)+(6*3)+(5*0)+(4*5)+(3*7)+(2*6)+(1*5)=83
83 % 10 = 3
So 13057-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O5/c1-14-8-4-2-3-5-9(8)15-6-7(11)10(12)13/h2-5,7,11H,6H2,1H3,(H,12,13)
13057-65-3Relevant articles and documents
PRODUCTION METHOD OF α-HYDROXYCARBOXYLIC ACID
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Paragraph 0042; 0075, (2016/10/07)
PROBLEM TO BE SOLVED: To provide an efficient production method of an α-hydroxycarboxylic acid in a mild condition, and to provide a production method of a biodegradable plastic from a raw material containing the α-hydroxycarboxylic acid. SOLUTION: In a synthesis method of an α-hydroxycarboxylic acid, which is a production method of the α-hydroxycarboxylic acid by oxidizing a 1,2-diol compound in a reaction system using a nitroxy radical including a skeleton represented by formula(1), water, and an organic solvent, the organic solvent is a compound unmixable with water (R1-R4 are respectively and independently 1-6C hydrocarbon groups). In the synthesis method of the α-hydroxycarboxylic acid, the reaction system has a pH value of 1.0-8.0, and includes a phosphate buffer solution or an acetate buffer solution, and at least one selected from a hypohalite and a halite is added to the reaction system, and further at least one selected from a tetraalkylammonium salt and a fatty acid is added thereto. COPYRIGHT: (C)2016,JPOandINPIT
Synthesis of enantiomerically pure 3-aryloxy-2-hydroxypropanoic acids, intermediate products in the synthesis of cis-4-Aminochroman-3-ols
Bredikhina,Pashagin,Kurenkov,Bredikhin
, p. 535 - 539 (2014/06/10)
Oxidation of accessible (R)-3-chloropropane-1,2-diol to (R)-3-chloro-2-hydroxypropanoic acid and subsequent reaction of the latter with ortho-substituted sodium phenoxide gave a number of enantiomerically pure 3-aryloxy-2-hydroxypropanoic acid which are intermediate products in the synthesis of nonracemic 4-aminochroman-3-ols.