1262015-07-5 Usage
General Description
(2S,3R)-3-hydroxy-1,2-Pyrrolidinedicarboxylic acid, 1-(phenylMethyl) ester is a chemical compound that is formed by the esterification of (2S,3R)-3-hydroxy-1,2-pyrrolidinedicarboxylic acid with phenylmethyl alcohol. It is often used as a building block in the synthesis of various pharmaceuticals and organic compounds. (2S,3R)-3-hydroxy-1,2-Pyrrolidinedicarboxylic acid, 1-(phenylMethyl) ester has a pyrrolidine ring with a hydroxy group and two carboxylic acid groups, making it a versatile intermediate for the synthesis of biologically active molecules. It is also known for its potential application in drug discovery and development due to its unique chemical structure and properties. Additionally, the phenylmethyl ester group in the compound provides additional reactivity and functionalization capabilities for further chemical modifications and derivatizations. Overall, this compound has significant importance in the field of medicinal chemistry and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 1262015-07-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,0,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1262015-07:
(9*1)+(8*2)+(7*6)+(6*2)+(5*0)+(4*1)+(3*5)+(2*0)+(1*7)=105
105 % 10 = 5
So 1262015-07-5 is a valid CAS Registry Number.
1262015-07-5Relevant articles and documents
D-Glucose based syntheses of β-hydroxy derivatives of l-glutamic acid, l-glutamine, l-proline and a dihydroxy pyrrolidine alkaloid
Kumar, K. S. Ajish,Chattopadhyay, Subrata
, p. 19455 - 19464 (2015/06/09)
The β-hydroxy derivatives of l-glutamic acid, l-glutamine and l-proline, useful for peptide/protein studies, were synthesized starting from d-glucose. The C2 carbon in d-glucose provided the carboxylic acid functionality, while the amino and β-hydroxy groups of the amino acids were amenable from the C3 and C4 hydroxy groups of the sugar, respectively. The key intermediate with appropriate carbon framework of the target molecules was constructed by homologation of a suitable azido-d-glucofuranose derivative using the Arndt-Eistert reaction. This journal is
