175476-93-4 Usage
Description
(1S,5R)-tert-Butyl 7-oxo-6-oxa-2-azabicyclo[3.2.1]octane-2-carboxylate is a bicyclic chemical compound with the molecular formula C12H19NO4. It features a lactone ring and an azabicyclo ring, with a tert-butyl group attached to the lactone ring and a carboxylate group attached to the azabicyclo ring. This unique structure and the presence of functional groups make it a promising candidate for pharmaceutical applications and further research in drug development and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
(1S,5R)-tert-Butyl 7-oxo-6-oxa-2-azabicyclo[3.2.1]octane-2-carboxylate is used as a potential pharmaceutical compound for its unique structure and functional groups. Its potential applications in drug development and medicinal chemistry are currently under investigation, with the aim of identifying its therapeutic properties and possible uses in treating various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 175476-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,7 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175476-93:
(8*1)+(7*7)+(6*5)+(5*4)+(4*7)+(3*6)+(2*9)+(1*3)=174
174 % 10 = 4
So 175476-93-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO4/c1-11(2,3)16-10(14)12-5-4-7-6-8(12)9(13)15-7/h7-8H,4-6H2,1-3H3/t7-,8+/m1/s1
175476-93-4Relevant articles and documents
Asymmetric synthesis of cis-4- and trans-3-hydroxypipecolic acids
Alegret, Carlos,Ginesta, Xavier,Riera, Antoni
experimental part, p. 1789 - 1796 (2009/04/07)
Enantioselective syntheses of cis-4- and trans-3-hydroxypipecolic acids from 2,3-epoxy-5-hexen-1-ol (7) are described. Regioselective C-3 or C-2 ring opening of the epoxide by the appropriate nitrogen nucleophile is the key step in each route. As enantiom
