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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)-

2-(1-benzylpiperidin-4-yl)propan-2-ol

CC(C1CCN(CC1)Cc1ccccc1)(O)C Request for Quotation
Chemical Name: 2-(1-benzylpiperidin-4-yl)propan-2-ol
CAS Number: 299428-04-9
Product Number: AG003EP5(AGN-PC-03NUZX)
Synonyms:
MDL No:
Molecular Formula: C15H23NO
Molecular Weight: 233.3492

Identification/Properties

Properties
BP:
331.052°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
233.355g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
233.178g/mol
Monoisotopic Mass:
233.178g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
225
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-(1-Benzylpiperidin-4-yl)-2-propanol plays a crucial role in chemical synthesis as a versatile intermediate. Its unique structural properties make it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. With its distinct piperidine and benzyl moieties, this compound serves as a key precursor for the synthesis of diverse complex organic molecules. Its ability to undergo multiple functional group transformations enables the generation of a wide range of derivatives with tailored properties. Through strategic manipulations of its chemical structure, researchers can access novel compounds with enhanced biological activities or desirable physicochemical characteristics. The application of 2-(1-Benzylpiperidin-4-yl)-2-propanol in chemical synthesis offers a pathway to explore new chemical space and develop innovative molecules with potential applications in drug discovery and material science.