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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, 1-ethyl-

CCN1CCC(CC1)O Request for Quotation
Chemical Name: 4-Piperidinol, 1-ethyl-
CAS Number: 3518-83-0
Product Number: AG003814(AGN-PC-0JLQG2)
Synonyms:
MDL No:
Molecular Formula: C7H15NO
Molecular Weight: 129.2001

Identification/Properties

Computed Properties
Molecular Weight:
129.203g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
129.115g/mol
Monoisotopic Mass:
129.115g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
77
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-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Ethyl-4-hydroxypiperidine, a versatile compound utilized in chemical synthesis, plays a crucial role in various reactions within the field of organic chemistry. This compound serves as a key building block in the creation of complex molecules and structures due to its unique chemical properties and reactivity. As a primary ingredient in numerous synthetic pathways, N-Ethyl-4-hydroxypiperidine enables the formation of diverse chemical bonds and functional groups, facilitating the development of pharmaceuticals, agrochemicals, and other specialty chemicals. Through its participation in coupling reactions, oxidation processes, and other transformative steps, this compound serves as a valuable tool for chemists seeking to construct intricate molecular frameworks with precision and efficiency.