17675-99-9 Usage
Uses
Used in Organic Synthesis:
(3R,4R)-3,4-dihydroxyoxolan-2-one is used as a versatile building block for the synthesis of various bioactive compounds. Its unique structure and stereochemistry allow for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Research:
(3R,4R)-3,4-dihydroxyoxolan-2-one is used as a key intermediate in the development of pharmaceuticals. Its specific stereochemical configuration may contribute to the compound's biological activities, making it a valuable asset in the search for new medications and therapies.
Used in the Pharmaceutical Industry:
(3R,4R)-3,4-dihydroxyoxolan-2-one is used as a precursor for the synthesis of pharmaceutical intermediates. Its unique properties and structure enable the development of new drugs with potential applications in treating various medical conditions.
Used in the Chemical Industry:
(3R,4R)-3,4-dihydroxyoxolan-2-one is used as a valuable compound in the chemical industry for the production of various chemical products. Its specific stereochemistry and versatile structure make it an attractive candidate for further research and development in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 17675-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,7 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17675-99:
(7*1)+(6*7)+(5*6)+(4*7)+(3*5)+(2*9)+(1*9)=149
149 % 10 = 9
So 17675-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O4/c5-2-1-8-4(7)3(2)6/h2-3,5-6H,1H2
17675-99-9Relevant academic research and scientific papers
A new efficient access to glycono-1,4-lactones by oxidation of unprotected itols by catalytic hydrogen transfer with RhH(PPh3)4-benzalacetone system
Isaac,Aizel,Stasik,Wadouachi,Beaupère
, p. 475 - 476 (2007/10/03)
Treatment of unprotected pentitols and hexitols with RhH(PPh3)4-benzalacetone system leads exclusively to glycono-1,4-lactones in 60-96% yield.
Autoxidation Reaction Mechanism for L-Ascorbic Acid-related Compounds in Methanol without Metal Ion Catalysis
Miyake, Noriko,Kurata, Tadao
, p. 811 - 813 (2007/10/03)
The autoxidation mechanism for L-ascorbic acid (ASA)-related compounds such as D-arabo-ascorbic acid (= erythorbic acid; ERA) and triose reductone (TR) in methanol without metal ion catalysis was studied.The oxidation reaction of these ASA-related compounds seems to proceed via the C(2) oxygen adduct of ERA (or TR) by a similar reaction mechanism to that of ASA. - Keywords: L-ascorbic acid; autoxidation; D-erythorbic acid; triose reductone; C(2) oxygen adduct
