327594-26-3 Usage
Description
(1S)-1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol is a chiral compound characterized by a complex structure that includes a furodioxol ring system and two hydroxyl groups attached to a central ethane moiety. The (1S) configuration denotes the specific stereochemistry of the molecule, which may influence its properties and potential applications.
Uses
Used in Pharmaceutical Industry:
(1S)-1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol is used as a potential pharmaceutical compound for its unique structural features and stereochemistry, which may contribute to specific biological activities and therapeutic effects.
Used as a Synthetic Intermediate:
In the field of organic chemistry, (1S)-1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]ethane-1,2-diol serves as a synthetic intermediate, facilitating the creation of more complex molecules and pharmaceutical agents through chemical reactions.
Used in Research and Development:
This chiral compound is also utilized as a research tool in organic chemistry, enabling scientists to study its properties, reactivity, and potential applications in various chemical processes and reactions. Further experimental studies and analysis are required to fully understand and exploit its capabilities.
Check Digit Verification of cas no
The CAS Registry Mumber 327594-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,5,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 327594-26:
(8*3)+(7*2)+(6*7)+(5*5)+(4*9)+(3*4)+(2*2)+(1*6)=163
163 % 10 = 3
So 327594-26-3 is a valid CAS Registry Number.
327594-26-3Relevant articles and documents
The role of the C-3 substituent in the asymmetric dihydroxylation of hexo-5-enofuranosides
Mereyala, Hari Babu,Goud, P. Mallikarjun,Gadikota, Rajendrakumar Reddy,Maddala, Rama Krishna,Reddy, K. Ramasubba
, p. 1201 - 1210 (2000)
Asymmetric dihydroxylation of vinyl furanosides 1-6 by use of OsO4, AD-mix-α and β is described yielding the corresponding hexofuranose sugars. Vinyl furanosides 2 and 3, with an ester group at C-3, and vinyl manno furanoside 5 on asymmetric dihydroxylation with AD-mix α exhibited high R diastereoselectivity at C-5. Reversal in diastereoselectivity at C-5 was observed for the 3-deoxy vinyl furanoside 6 giving furanosaccharide 6S with the S configuration at C-5.
