356073-54-6 Usage
General Description
(7S)-1,4-dioxa-8-azaspiro[4.5]decane-7-carboxylic acid is a chemical compound with a complex and specific structure. It is classified as a spiro compound, meaning it contains a spiro bridge that connects two non-adjacent atoms. The presence of the carboxylic acid group indicates that it is a carboxylic acid, which is a functional group consisting of a carbon atom double bonded to an oxygen atom and also bonded to a hydroxyl group. (7S)-1,4-dioxa-8-azaspiro[4.5]decane-7-carboxylic acid contains a 7S stereochemistry, indicating the spatial arrangement of the substituents around the seventh atom in the structure. The compound's specific structure and stereochemistry give it unique properties and potential pharmaceutical or chemical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 356073-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,0,7 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 356073-54:
(8*3)+(7*5)+(6*6)+(5*0)+(4*7)+(3*3)+(2*5)+(1*4)=146
146 % 10 = 6
So 356073-54-6 is a valid CAS Registry Number.
356073-54-6Relevant articles and documents
Asymmetric syntheses of enantiopure 4-substituted pipecolic acid derivatives
Agami, Claude,Bisaro, Fabrice,Comesse, Sebastien,Guesne, Sebastien,Kadouri-Puchot, Catherine,Morgentin, Remy
, p. 2385 - 2389 (2007/10/03)
(2R,4R)-4-Methylpipecolic acid and (2S,4R)-4-hydroxypipecolic acid, two biologically active amino acids, were synthesized using the same strategy. A third amino acid, obtained in a protected form, was also obtained in the same way. The key step of these syntheses involves an intramolecular eneiminium cyclization which occurs with complete stereoselectivity. The resulting exocyclic double bond can react in a diastereoselective way to afford pure lactones, which can then be efficiently converted into the amino acids.
