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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)-

1-Pyrrolidineethanamine, a-(phenylmethyl)-, (aS)-

N[C@@H](Cc1ccccc1)CN1CCCC1 Request for Quotation
Chemical Name: 1-Pyrrolidineethanamine, a-(phenylmethyl)-, (aS)-
CAS Number: 200267-75-0
Product Number: AG002CN4(AGN-PC-0QR85V)
Synonyms:
MDL No:
Molecular Formula: C13H20N2
Molecular Weight: 204.3113

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3259
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-1-Phenyl-3-(pyrrolidin-1-yl)propan-2-amine compound, also known as $name$, is a versatile molecule widely utilized in chemical synthesis processes. This compound plays a crucial role as a chiral building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structural configuration and reactivity make it a valuable tool for the controlled synthesis of complex molecules with specific chirality.In chemical synthesis, (S)-1-Phenyl-3-(pyrrolidin-1-yl)propan-2-amine serves as a key intermediate in the production of enantiopure compounds. Its chirality allows for the precise control of stereochemistry in the construction of asymmetrical carbon centers, essential for designing bioactive molecules with high selectivity and potency. This compound is often incorporated into the synthesis of advanced drug candidates, where the arrangement of atoms in three-dimensional space significantly impacts biological activity and interactions within biological systems.Furthermore, the utilization of (S)-1-Phenyl-3-(pyrrolidin-1-yl)propan-2-amine in chemical synthesis extends beyond pharmaceutical applications. It finds use in the production of fine chemicals, functional materials, and other high-value compounds requiring chirality control for optimal performance. The strategic incorporation of this compound into synthetic routes enables chemists to access a diverse range of enantiomerically pure products, opening up possibilities for innovative drug discovery, material science, and chemical research.