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

O[C@H]1CCCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 3-Piperidinol, 1-(phenylmethyl)-, (3S)-
CAS Number: 91599-79-0
Product Number: AG003CJQ(AGN-PC-0OMRRC)
Synonyms:
MDL No:
Molecular Formula: C12H17NO
Molecular Weight: 191.2695

Identification/Properties

Properties
BP:
296.8°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
191.274g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-Benzylpiperidin-3-ol, also known as $name$, is a valuable compound widely utilized in various chemical synthesis applications. As a chiral building block, it plays a crucial role in the creation of pharmaceuticals, agrochemicals, and advanced materials. The presence of a piperidine ring and a benzyl group in its structure imparts unique reactivity, making it a versatile compound for the formation of complex molecules. In particular, (S)-1-Benzylpiperidin-3-ol is commonly employed in the synthesis of biologically active compounds due to its ability to introduce chirality and influence the stereochemistry of the final products. Its strategic incorporation into organic reactions enables the development of novel molecules with enhanced properties and functionalities. By serving as a key intermediate in chemical transformations, (S)-1-Benzylpiperidin-3-ol contributes significantly to the advancement of synthetic methodologies and the discovery of innovative compounds in various research fields.