103290-40-0 Usage
General Description
(2S,4R)-4-Phenylpyrrolidine-2-carboxylic acid is a chemical compound belonging to the pyrrolidine and carboxylic acid families. It is a chiral molecule, meaning it has a non-superimposable mirror image. (2S,4R)-4-PHENYLPYRROLIDINE-2-CARBOXYLIC ACID has potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. It may also be used as a building block in organic synthesis, particularly in the creation of new chemical entities for drug discovery and development. Additionally, the phenyl group in its structure confers certain properties that may make it suitable for use in materials science and other industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 103290-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,9 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103290-40:
(8*1)+(7*0)+(6*3)+(5*2)+(4*9)+(3*0)+(2*4)+(1*0)=80
80 % 10 = 0
So 103290-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO2/c13-11(14)10-6-9(7-12-10)8-4-2-1-3-5-8/h1-5,9-10,12H,6-7H2,(H,13,14)/t9-,10-/m0/s1
103290-40-0Relevant articles and documents
Macrocyclic inhibitors of the PD-1/PD-L1 and CD80(B7-1)/PD-L1 protein/protein interactions
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Page/Page column 1675; 1676, (2016/05/09)
The present disclosure provides novel macrocyclic peptides which inhibit the PD-1/PD-L1 and PD-L1/CD80 protein/protein interaction, and thus are useful for the amelioration of various diseases, including cancer and infectious diseases.
LITHIUM DIPHENYLCUPRATE REACTIONS WITH 4-TOSYLOXY-L-PROLINES; AN INTERESTING STEREOCHEMICAL OUTCOME. A SYNTHESIS OF TRANS-4-PHENYL-L-PROLINE.
Thottathil, John K.,Moniot, Jerome L.
, p. 151 - 154 (2007/10/02)
The reaction of lithium diphenylcuprate with trans-4- and cis-4-tosyloxy-L-prolines gives excellent yields of 4-phenyl substituted L-prolines and the reaction proceeds with net retention of configuration at the carbon center bearing the tosyloxy group.