1262015-07-5 Usage
Description
(2S,3R)-3-hydroxy-1,2-Pyrrolidinedicarboxylic acid, 1-(phenylMethyl) ester is a versatile chemical compound formed by the esterification of (2S,3R)-3-hydroxy-1,2-pyrrolidinedicarboxylic acid with phenylmethyl alcohol. It features a pyrrolidine ring with a hydroxy group and two carboxylic acid groups, making it a valuable intermediate for the synthesis of biologically active molecules. The phenylmethyl ester group in the compound enhances its reactivity and functionalization capabilities, contributing to its significance in medicinal chemistry and organic synthesis.
Uses
Used in Pharmaceutical Synthesis:
(2S,3R)-3-hydroxy-1,2-Pyrrolidinedicarboxylic acid, 1-(phenylMethyl) ester is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure and properties make it a promising candidate for drug discovery and development.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2S,3R)-3-hydroxy-1,2-Pyrrolidinedicarboxylic acid, 1-(phenylMethyl) ester is utilized as a versatile intermediate for the synthesis of biologically active molecules, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
(2S,3R)-3-hydroxy-1,2-Pyrrolidinedicarboxylic acid, 1-(phenylMethyl) ester is employed as a key intermediate in organic synthesis, allowing for the creation of a wide range of chemical compounds and materials.
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
