62445-25-4 Usage
Description
(S)-2,4-Dihydroxybutyric acid, also known as (S)-2,4-DHB, is a naturally occurring chiral organic compound that belongs to the class of hydroxybutyric acids. It is the biologically active (S)-enantiomer and is found in certain plant tissues. (S)-2,4-DHB plays a key role in the biosynthesis of vitamin C and exhibits antioxidant properties. Its potential therapeutic effects in treating various diseases, such as cancer and neurodegenerative disorders, make it an important target for biochemical studies and pharmaceutical research.
Uses
Used in Pharmaceutical Industry:
(S)-2,4-DHB is used as a key intermediate in the biosynthesis of vitamin C, which is essential for various physiological functions and maintaining overall health.
(S)-2,4-DHB is used as a potential therapeutic agent for the treatment of various diseases, including cancer and neurodegenerative disorders, due to its antioxidant properties and potential therapeutic effects.
Used in Biochemical Research:
(S)-2,4-DHB is used as an important target for biochemical studies, as its chiral nature and biological activity provide valuable insights into the structure-function relationships of organic compounds and their potential applications in medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 62445-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,4 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62445-25:
(7*6)+(6*2)+(5*4)+(4*4)+(3*5)+(2*2)+(1*5)=114
114 % 10 = 4
So 62445-25-4 is a valid CAS Registry Number.
62445-25-4Relevant articles and documents
A METHOD OF PRODUCTION OF ２,4-DIHYDROXYBUTYRIC ACID
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Page/Page column 1, (2017/01/05)
A method for the preparation of 2,4-dihydroxybutyric acid (2,4-DHB) including the successive steps of converting malate, succinyl-CoA and/or glyoxylate into malyl-CoA, converting malyl-CoA previously obtained into malate-4-semialdehyde, and converting malate-4-semialdehyde into 2,4-DHB using a DHB dehydrogenase.
Synthesis and Nuclear Magnetic Resonance Studies of Some N-Acylated Methyl 4-Amino-4,6-dideoxy-α-D-mannopyranosides
Kenne, Lennart,Unger, Per,Wehler, Thomas
, p. 1183 - 1186 (2007/10/02)
The methyl α-glycosides of 4-amino-4,6-dideoxy-D-mannopyranose (perosamine), N-acylated with either formic, acetic, or (S)-2,4-dihydroxybutanoic acid, have been synthesized.The (1)H and (13)C n.m.r. spectra of these substances and the parent, non-N-acylated glycoside, demonstrated how the chemical shifts are influenced by the N-acylation.The N-formyl derivative occured in two conformations, s-cis and s-trans, and the free-energy barrier between these, 86.9 kJ mol-1, was defined by dynamic n.m.r. spectroscopy.
