1. Home
  2. 3-Piperidinemethanol, 1-(phenylmethyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, 1-(phenylmethyl)-

OCC1CCCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 3-Piperidinemethanol, 1-(phenylmethyl)-
CAS Number: 85387-44-6
Product Number: AG004KQP(AGN-PC-05WVPC)
Synonyms:
MDL No:
Molecular Formula: C13H19NO
Molecular Weight: 205.2961

Identification/Properties

Properties
BP:
294.068 °C at 760 mmHg
Computed Properties
Molecular Weight:
205.301g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
205.147g/mol
Monoisotopic Mass:
205.147g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
177
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


1-(Phenylmethyl)-3-piperidinemethanol is a versatile compound used in chemical synthesis as a key building block for creating a variety of more complex molecules. Due to its unique structure, it serves as a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. With its piperidine ring providing stability and reactivity, this compound is employed in the synthesis of various bioactive compounds and heterocycles. Its presence in the molecular structure can enhance biological activity, making it a crucial component in the development of new drugs and therapeutic agents. In addition, its ability to undergo diverse chemical transformations makes it a valuable tool for organic chemists in the creation of novel compounds with specific properties and functions.