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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)-N-(Pyrrolidin-3-yl)acetamide hydrochloride

CC(=O)N[C@@H]1CNCC1.Cl Request for Quotation
Chemical Name: (S)-N-(Pyrrolidin-3-yl)acetamide hydrochloride
CAS Number: 1246277-44-0
Product Number: AG0074H3(AGN-PC-0WAHHV)
Synonyms:
MDL No:
Molecular Formula: C6H13ClN2O
Molecular Weight: 164.6332

Identification/Properties

Computed Properties
Molecular Weight:
164.633g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
164.072g/mol
Monoisotopic Mass:
164.072g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
114
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-N-(Pyrrolidin-3-yl)acetamide hydrochloride is a versatile compound commonly utilized in chemical synthesis as a chiral building block. This compound plays a crucial role in asymmetric synthesis, providing a way to introduce chirality into various molecular structures. By incorporating (S)-N-(Pyrrolidin-3-yl)acetamide hydrochloride into a reaction, chemists can selectively create enantiomerically pure products, leading to compounds with specific biological activity or pharmacological properties. Additionally, this compound can serve as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, making it an essential component in modern organic chemistry research and development.