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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)-Pyrrolidine-2-carboxamide hydrochloride

NC(=O)[C@@H]1CCCN1.Cl Request for Quotation
Chemical Name: (S)-Pyrrolidine-2-carboxamide hydrochloride
CAS Number: 42429-27-6
Product Number: AG003CO9(AGN-PC-0WAFXX)
Synonyms:
MDL No:
Molecular Formula: C5H11ClN2O
Molecular Weight: 150.6066

Identification/Properties

Properties
MP:
178-182 °C
BP:
303.6°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-Pyrrolidine-2-carboxamide hydrochloride possesses versatile applications in chemical synthesis, particularly in the realm of pharmaceutical and agrochemical industries. This compound serves as a vital chiral building block, enabling organic chemists to introduce specific chirality into complex molecules with precision and efficacy. The presence of a pyrrolidine ring in its structure imparts unique reactivity, making it a key component in the synthesis of various pharmaceutical intermediates and active compounds. As a potent catalyst, (S)-Pyrrolidine-2-carboxamide hydrochloride facilitates asymmetric transformations, allowing for the creation of enantiomerically pure compounds essential in drug discovery and development. Its role in organic synthesis extends to the preparation of chiral ligands, asymmetric reagents, and other valuable compounds used in the synthesis of biologically active molecules. This compound's significance lies in its ability to steer chemical reactions towards the desired enantiomeric outcome, making it an indispensable tool in the hands of synthetic chemists striving to create intricate molecular structures with high stereochemical control.