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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)-

4-Piperidinol, 3-methyl-1-(phenylmethyl)-

OC1CCN(CC1C)Cc1ccccc1 Request for Quotation
Chemical Name: 4-Piperidinol, 3-methyl-1-(phenylmethyl)-
CAS Number: 91600-19-0
Product Number: AG00H30B(AGN-PC-00NAH1)
Synonyms:
MDL No:
Molecular Formula: C13H19NO
Molecular Weight: 205.29606

Identification/Properties

Computed Properties
Molecular Weight:
205.301g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
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:
189
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Benzyl-3-methylpiperidin-4-ol, a versatile organic compound, finds wide application in the realm of chemical synthesis due to its unique structural properties. Acting as a key intermediate in various synthesis pathways, this compound serves as a crucial building block for the production of diverse pharmaceuticals, agrochemicals, and specialty chemicals. Its role in the synthesis of complex molecules is particularly noteworthy, as it imparts specific functional groups and stereochemical features essential for target molecule formation. Additionally, 1-Benzyl-3-methylpiperidin-4-ol facilitates the creation of novel compounds with enhanced biological activities and tailored physical properties, making it a valuable tool in the hands of synthetic chemists striving to innovate and advance the field of organic chemistry.