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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

(R)-1-Methylpyrrolidine-3-carboxylic acid

CN1CC[C@H](C1)C(=O)O Request for Quotation
Chemical Name: (R)-1-Methylpyrrolidine-3-carboxylic acid
CAS Number: 952484-55-8
Product Number: AG00IIVY(AGN-PC-0WAI5H)
Synonyms:
MDL No:
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-1-Methylpyrrolidine-3-carboxylic acid is a versatile compound commonly utilized in chemical synthesis as a chiral building block. Its unique structure and chirality make it a valuable precursor for the preparation of enantiopure compounds in various chemical reactions. The presence of a pyrrolidine ring and a carboxylic acid group allows for efficient functionalization, enabling the synthesis of complex molecules with defined stereochemistry. This compound is particularly valuable in the pharmaceutical industry for the preparation of enantiomerically pure drug candidates, as well as in the production of fine chemicals and agrochemicals. Its application in asymmetric synthesis and as a ligand in catalytic reactions highlights its significance in modern organic chemistry.