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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)-

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

CN1CC[C@@H](C1)C(=O)O Request for Quotation
Chemical Name: (S)-1-Methylpyrrolidine-3-carboxylic acid
CAS Number: 952484-58-1
Product Number: AG003A84(AGN-PC-0WAI5I)
Synonyms:
MDL No:
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Computed Properties
Molecular Weight:
129.159g/mol
XLogP3:
-2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
129.079g/mol
Monoisotopic Mass:
129.079g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
124
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-Methylpyrrolidine-3-carboxylic acid is a valuable compound widely utilized in chemical synthesis processes. This chiral compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural properties and versatile reactivity.In chemical synthesis, (S)-1-Methylpyrrolidine-3-carboxylic acid can be employed as a precursor for the synthesis of enantiopure compounds, especially in the pharmaceutical industry where the stereochemistry of molecules plays a significant role in their biological activity and pharmacokinetic properties. By incorporating this compound into synthetic pathways, chemists can access enantiomerically pure products with high selectivity and efficiency.Furthermore, (S)-1-Methylpyrrolidine-3-carboxylic acid can act as a ligand in catalytic reactions, enabling the formation of complex molecules with precise stereochemistry under mild conditions. Its ability to engage in various bond-forming reactions makes it a valuable tool for designing and optimizing synthetic routes in the development of new chemical entities.Overall, the use of (S)-1-Methylpyrrolidine-3-carboxylic acid in chemical synthesis offers chemists a powerful means to access enantiopure compounds and efficiently construct complex molecular frameworks with controlled stereochemistry, making it an indispensable component in the toolkit of synthetic chemists across different industries.