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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-Benzyl-4,4-difluoropiperidin-3-yl)methanol

OCC1CN(CCC1(F)F)Cc1ccccc1 Request for Quotation
Chemical Name: (1-Benzyl-4,4-difluoropiperidin-3-yl)methanol
CAS Number: 1303973-25-2
Product Number: AG00HS1D(AGN-PC-0WCBY4)
Synonyms:
MDL No: MFCD18909828
Molecular Formula: C13H17F2NO
Molecular Weight: 241.2770

Identification/Properties

Computed Properties
Molecular Weight:
241.282g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
241.128g/mol
Monoisotopic Mass:
241.128g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
242
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 4,4-Difluoro-1-(phenylmethyl)-3-piperidinemethanol finds widespread application in chemical synthesis as a versatile building block. Its unique structural features make it a valuable intermediate in the creation of various organic compounds, particularly in pharmaceutical and agrochemical industries. In chemical synthesis, this compound serves as a key component for the preparation of complex molecules due to its ability to undergo diverse reactions and functionalizations. It can be utilized for the synthesis of novel drugs, pesticides, and other biologically active compounds. Additionally, the presence of both a fluorine atom and a phenylmethyl group enhances the reactivity and specificity of this molecule in various synthetic pathways.With its strategic placement of functional groups, 4,4-Difluoro-1-(phenylmethyl)-3-piperidinemethanol enables chemists to introduce specific structural motifs with precision, facilitating the creation of molecules with desired properties. Its inclusion in chemical reactions can lead to the formation of stereochemically complex compounds, making it a valuable tool for synthetic chemists aiming to access structurally diverse compounds for various applications.