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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-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4S)-

OC[C@H]1CN(C)CC[C@@H]1c1ccc(cc1)F Request for Quotation
Chemical Name: 3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl-, (3R,4S)-
CAS Number: 389573-45-9
Product Number: AG00C92J(AGN-PC-0O9QIF)
Synonyms:
MDL No:
Molecular Formula: C13H18FNO
Molecular Weight: 223.2865232

Identification/Properties

Properties
MP:
98-100°C
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
223.291g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
223.137g/mol
Monoisotopic Mass:
223.137g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
216
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound ((3R,4S)-4-(4-Fluorophenyl)-1-methylpiperidin-3-yl)methanol is a versatile building block in chemical synthesis due to its unique structural characteristics. It can serve as a key intermediate in the preparation of various pharmaceuticals and fine chemicals. Specifically, this compound can be utilized as a chiral synthon in the synthesis of complex molecules with high stereochemical control. Its piperidine ring confers steric and electronic properties that enable selective functional group transformations, making it a valuable component in the development of new synthetic routes. Furthermore, the presence of a fluorophenyl group enhances the compound's reactivity and allows for further diversification through various coupling reactions. The resulting products can exhibit enhanced biological activity or specific molecular recognition properties, making this compound a valuable tool in the arsenal of synthetic chemists.