1. Home
  2. 2-Pyrrolidinecarboxamide, 1-(chloroacetyl)-, (2S)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

2-Pyrrolidinecarboxamide, 1-(chloroacetyl)-, (2S)-

ClCC(=O)N1CCC[C@H]1C(=O)N Request for Quotation
Chemical Name: 2-Pyrrolidinecarboxamide, 1-(chloroacetyl)-, (2S)-
CAS Number: 214398-99-9
Product Number: AG00BG7C(AGN-PC-0O7UQZ)
Synonyms:
MDL No:
Molecular Formula: C7H11ClN2O2
Molecular Weight: 190.6274

Identification/Properties

Computed Properties
Molecular Weight:
190.627g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
190.051g/mol
Monoisotopic Mass:
190.051g/mol
Topological Polar Surface Area:
63.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
208
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(S)-1-(2-Chloroacetyl)pyrrolidine-2-carboxamide, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various complex molecules due to its unique chemical properties. In synthetic organic chemistry, (S)-1-(2-Chloroacetyl)pyrrolidine-2-carboxamide is frequently employed as a chiral reagent for asymmetric reactions, allowing for the selective formation of enantiomerically pure products. Its ability to introduce chirality into molecules makes it a valuable tool in the pharmaceutical industry for the synthesis of enantiomerically pure drug compounds. Additionally, (S)-1-(2-Chloroacetyl)pyrrolidine-2-carboxamide is utilized in the preparation of peptide structures and in the development of novel chemical entities with potential biological activity. Its diverse applications in chemical synthesis highlight its significance as a crucial intermediate for the construction of complex molecular architectures with precise stereochemical control.