475504-32-6 Usage
General Description
(2R,4R)-4-hydroxypipecolic acid methyl ester is a chemical compound that belongs to the class of pipecolic acid derivatives. It has a molecular structure with a hydroxyl group attached to the fourth and a methyl ester group attached to the carboxylic acid functional group. (2R,4R)-4-hydroxypipecolic acid methyl ester has potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of biologically active molecules. It may also have uses in agricultural and environmental science due to its potential role in plant-microbe interactions and its ability to act as a signaling molecule in plants. Furthermore, (2R,4R)-4-hydroxypipecolic acid methyl ester's stereochemistry makes it an important chiral compound, with potential applications in asymmetric synthesis and drug development. Overall, this chemical compound has diverse potential uses across various fields of science and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 475504-32-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,5,0 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 475504-32:
(8*4)+(7*7)+(6*5)+(5*5)+(4*0)+(3*4)+(2*3)+(1*2)=156
156 % 10 = 6
So 475504-32-6 is a valid CAS Registry Number.
475504-32-6Relevant articles and documents
Use of hydrolases for the synthesis of cyclic amino acids
Lloyd, Richard C.,Lloyd, Michael C.,Smith, Mark E. B.,Holt, Karen E.,Swift, Jonathan P.,Keene, Philip A.,Taylor, Stephen J. C.,McCague, Raymond
, p. 717 - 728 (2007/10/03)
The synthesis of several cyclic amino acids that have all the necessary structural features to make them ideal scaffolds for use in medicinal chemistry is described. A key step in each synthesis is the use of hydrolase enzymes to define a chiral centre. I
Novel constrained CCK-B dipeptoid antagonists derived from pipecolic acid
Bellier, Bruno,Da Nascimento, Sophie,Meudal, Herve,Gincel, Edith,Roques, Bernard P.,Garbay, Christiane
, p. 1419 - 1424 (2007/10/03)
A new series of 4-substituted pipecolic acid derivatives was prepared and incorporated into dipeptoids. The resulting products behave as moderately potent CCK-B antagonists but their constrained structure and its comparison with structurally related compounds yield valuable information about the conformational requirements for optimal recognition of the CCK-B receptor by antagonists.
