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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)-tert-Butyl 2-acetylpyrrolidine-1-carboxylate

CC(=O)[C@@H]1CCCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: (S)-tert-Butyl 2-acetylpyrrolidine-1-carboxylate
CAS Number: 91550-08-2
Product Number: AG00H2ZS(AGN-PC-0WAITE)
Synonyms:
MDL No:
Molecular Formula: C11H19NO3
Molecular Weight: 213.2735

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
213.277g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
213.136g/mol
Monoisotopic Mass:
213.136g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
268
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#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-tert-Butyl 2-acetylpyrrolidine-1-carboxylate is a versatile compound widely used in chemical synthesis. As a chiral building block, it plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science. Its asymmetric nature allows for precise control over stereochemistry in reactions, making it a valuable tool for creating complex molecular structures with high efficiency and selectivity. In asymmetric synthesis, this compound serves as a key starting material for the preparation of enantiomerically pure molecules, which is essential for drug discovery and development. Additionally, (S)-tert-Butyl 2-acetylpyrrolidine-1-carboxylate can be utilized in the synthesis of natural products, fine chemicals, and advanced materials, showcasing its broad applicability in modern organic chemistry.