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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)-

3-Pyrrolidinemethanol, 1-(phenylmethyl)-, (3S)-

OC[C@H]1CCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 3-Pyrrolidinemethanol, 1-(phenylmethyl)-, (3S)-
CAS Number: 78914-69-9
Product Number: AG005OBD(AGN-PC-0OI6O2)
Synonyms:
MDL No:
Molecular Formula: C12H17NO
Molecular Weight: 191.2695

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
191.274g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
191.131g/mol
Monoisotopic Mass:
191.131g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
166
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-(1-Benzylpyrrolidin-3-yl)methanol, also known as $name$, is a versatile compound widely used in chemical synthesis. Its chiral nature makes it an excellent building block for the preparation of enantiopure compounds, which are crucial in various fields such as pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, (S)-(1-Benzylpyrrolidin-3-yl)methanol serves as a valuable starting material for the synthesis of pharmaceutical drugs through asymmetric synthesis. Its chirality allows for the production of enantiomerically pure drug molecules, which often exhibit distinct biological activities compared to their racemic mixtures. By utilizing (S)-(1-Benzylpyrrolidin-3-yl)methanol as a chiral auxiliary or a key intermediate, chemists can efficiently access a wide range of chiral compounds with tailored properties.Furthermore, (S)-(1-Benzylpyrrolidin-3-yl)methanol can be employed in the synthesis of natural products, functional materials, and advanced organic molecules. Its presence in the synthetic toolbox enables chemists to access complex molecular architectures with high stereoselectivity, paving the way for the development of novel compounds with enhanced properties and applications.Overall, (S)-(1-Benzylpyrrolidin-3-yl)methanol is a valuable reagent in chemical synthesis, offering chemists a powerful tool to access enantiomerically pure compounds and drive innovation in diverse scientific fields.