6631-53-4 Usage
General Description
The chemical (1S,2R)-1-(2-phenyl-2H-1,2,3-triazol-4-yl)propane-1,2,3-triol is a compound that consists of a triazolyl group attached to a propane-1,2,3-triol backbone. It is an optically active molecule with one stereocenter at the first carbon and a chiral center at the second carbon. The phenyl group attached to the triazolyl ring provides aromatic character to the compound, while the triol moiety imparts hydrophilicity to the molecule. (1S,2R)-1-(2-phenyl-2H-1,2,3-triazol-4-yl)propane-1,2,3-triol may have potential applications in medicinal chemistry, as well as in the development of novel materials due to its unique structural features. Further research is needed to fully explore the potential uses and properties of (1S,2R)-1-(2-phenyl-2H-1,2,3-triazol-4-yl)propane-1,2,3-triol.
Check Digit Verification of cas no
The CAS Registry Mumber 6631-53-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6631-53:
(6*6)+(5*6)+(4*3)+(3*1)+(2*5)+(1*3)=94
94 % 10 = 4
So 6631-53-4 is a valid CAS Registry Number.
6631-53-4Relevant articles and documents
Highly efficient and selective biocatalytic acylation studies on triazolylsugars
Bhattacharya, Anupam,Prasad, Ashok K.,Maity, Jyotirmoy,Himanshu,Poonam,Olsen, Carl E.,Gross, Richard A.,Parmar, Virinder S.
, p. 10269 - 10277 (2007/10/03)
Different acid anhydrides (of C2 to C7 aliphatic fatty acids and benzoic acid) have been used to study the selective acylation of primary/secondary hydroxyl groups in 2-phenyl-4-(D-threo-1′,2′, 3′-trihydroxypropyl)-2H-1,2,3-triazole, 2-phenyl-4-(D-erythro-1′, 2′,3′-trihydroxypropyl)-2H-1,2,3-triazole, 2-phenyl-4-(D-arabino- 1′,2′,3′,4′-tetrahydroxybutyl)-2H-1,2,3-triazole and 2-phenyl-4-(D-lyxo-1′,2′,3′,4′-tetrahydroxybutyl)-2H-1, 2,3-triazole in the presence of Candida antarctica lipase B in diisopropyl ether. Among the different acid anhydrides, butanoic anhydride was found to be the most efficient acylating agent (for butanoylation); for acetylation, vinyl acetate gave the best results. The reactions with both these acylating agents were highly selective and efficient yielding exclusively the monoacylated products in 95-99% yields in 1-5 h.