20016-85-7 Usage
Description
(R)-2-Hydroxybutyric Acid, also known as (R)-2-HB, is an optically active form of 2-hydroxybutyric acid with an (R)-configuration. It is a chiral molecule that exists in two different forms, (R) and (S), which are mirror images of each other. The (R)-2-Hydroxybutyric Acid has unique properties and applications due to its specific configuration.
Uses
Used in Pharmaceutical Industry:
(R)-2-Hydroxybutyric Acid is used as a remedy for hangovers, helping to alleviate the symptoms and promote recovery. It is believed to work by increasing the body's metabolism of alcohol, thus reducing the severity and duration of hangover effects.
Used in Sports and Fitness Industry:
(R)-2-Hydroxybutyric Acid is used as a supplement to enhance physical performance and endurance. It is thought to improve energy levels and reduce fatigue during exercise, making it a popular choice among athletes and fitness enthusiasts.
Used in Research and Development:
(R)-2-Hydroxybutyric Acid is used in scientific research as a chiral building block for the synthesis of various pharmaceutical compounds. Its unique (R)-configuration allows for the development of new drugs with specific properties and applications.
Used in Cosmetics Industry:
(R)-2-Hydroxybutyric Acid may be used in the development of cosmetic products, particularly those targeting skin health and rejuvenation. Its potential benefits in this area are still being explored and researched.
Check Digit Verification of cas no
The CAS Registry Mumber 20016-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,1 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20016-85:
(7*2)+(6*0)+(5*0)+(4*1)+(3*6)+(2*8)+(1*5)=57
57 % 10 = 7
So 20016-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7)/t3-/m1/s1
20016-85-7Relevant articles and documents
Asymmetric Allylation and Reduction on an Ephedrine-Derived Template: Stereoselective Synthesis of α-Hydroxy Acids and Derivatives
Pansare, Sunil V.,Ravi, R.Gnana,Jain, Rajendra P.
, p. 4120 - 4124 (2007/10/03)
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A Novel Bicyclic Orthoester as a Chiral Auxiliary: Application to the Synthesis of α-Hydroxy Acids
Dube, D.,Deschenes, D.,Tweddell, J.,Gagnon, H.,Carlini, R.
, p. 1827 - 1830 (2007/10/02)
Chiral α-keto orthoesters derived from tartanic acid can be reduced diastereoselectively.Hydrolysis affords optically actice α-hydroxy acids and the recovered auxiliary.
