32359-20-9 Usage
Description
(1S,2R)-1,2-Dihydroxycyclohexa-3,5-diene-1-carboxylic acid is a chiral carboxylic acid with a unique cyclohexane ring structure, featuring two hydroxyl groups at the 1 and 2 positions and a carboxylic acid group at the 1 position. Its specific stereochemistry, denoted by the (1S,2R) prefix, makes it a rare and intriguing compound for research and development in the fields of organic synthesis and medicinal chemistry.
Uses
Used in Organic Synthesis:
(1S,2R)-1,2-Dihydroxycyclohexa-3,5-diene-1-carboxylic acid is used as a key intermediate in the synthesis of various organic compounds due to its unique structure and functional groups.
Used in Medicinal Chemistry:
(1S,2R)-1,2-Dihydroxycyclohexa-3,5-diene-1-carboxylic acid is used as a building block for the development of pharmaceuticals, taking advantage of its specific stereochemistry and functional groups to create novel drug candidates with potential therapeutic applications.
Used in Research and Development:
(1S,2R)-1,2-Dihydroxycyclohexa-3,5-diene-1-carboxylic acid serves as an interesting target for chemical research, enabling scientists to explore its properties, reactivity, and potential applications in various chemical and biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 32359-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,5 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32359-20:
(7*3)+(6*2)+(5*3)+(4*5)+(3*9)+(2*2)+(1*0)=99
99 % 10 = 9
So 32359-20-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O4/c8-5-3-1-2-4-7(5,11)6(9)10/h1-5,8,11H,(H,9,10)/t5-,7+/m1/s1
32359-20-9Relevant articles and documents
Palladium Catalyzed Stereoselective Arylation of Biocatalytically Derived Cyclic 1,3-Dienes: Chirality Transfer via a Heck-Type Mechanism
Dun?s, Petter,Kann, Nina,Kociok-K?hn, Gabriele,Lewis, Simon E.,Norrby, Per-Ola,Paterson, Andrew J.,Rahm, Martin
supporting information, p. 2464 - 2469 (2020/08/05)
Microbial arene oxidation of benzoic acid with Ralstonia eutropha B9 provides a chiral highly functionalized cyclohexadiene, suitable for further structural diversification. Subjecting this scaffold to a Pd-catalyzed Heck reaction effects a regio-and ster
A Formal Approach to Xylosmin and Flacourtosides E and F: Chemoenzymatic Total Synthesis of the Hydroxylated Cyclohexenone Carboxylic Acid Moiety of Xylosmin
Ghavre, Mukund,Froese, Jordan,Murphy, Brennan,Simionescu, Razvan,Hudlicky, Tomas
supporting information, p. 1156 - 1159 (2017/03/14)
The hydroxylated cyclohexenone carboxylic acid moiety of xylosmin was synthesized in eight steps from benzoic acid. The key steps in the synthesis involved the enzymatic dihydroxylation of benzoic acid by the whole cell fermentation with Ralstonia eutroph
Chemoenzymatic synthesis of idesolide from benzoic acid
Adams, David R.,Aichinger, Christian,Rinner, Uwe,Hudlicky, Tomas
body text, p. 725 - 729 (2011/04/26)
Idesolide was synthesized in five steps from benzoic acid by base-catalyzed dimerization of hydroxy keto ester, obtained from diol, the product of the whole-cell fermentation of benzoic acid with R. eutrophus B9. Georg Thieme Verlag Stuttgart - New York.