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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)-

Phenol, 3-(1-piperidinyl)-

Oc1cccc(c1)N1CCCCC1 Request for Quotation
Chemical Name: Phenol, 3-(1-piperidinyl)-
CAS Number: 27292-50-8
Product Number: AG00BG34(AGN-PC-0JO8DI)
Synonyms:
MDL No:
Molecular Formula: C11H15NO
Molecular Weight: 177.2429

Identification/Properties

Computed Properties
Molecular Weight:
177.247g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
177.115g/mol
Monoisotopic Mass:
177.115g/mol
Topological Polar Surface Area:
23.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
154
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Piperidin-1-yl)phenol, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structural properties. This compound finds application in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive phenolic group enables it to participate in a range of chemical reactions, such as nucleophilic substitutions, oxidations, and coupling reactions. In medicinal chemistry, 3-(Piperidin-1-yl)phenol is utilized for the synthesis of novel drug candidates targeting diseases like cancer, infectious diseases, and neurological disorders.Furthermore, its piperidine ring imparts steric hindrance and can modulate the compound's biological activity, making it a valuable scaffold for designing bioactive molecules with improved pharmacokinetic properties. In organic synthesis, 3-(Piperidin-1-yl)phenol serves as a key intermediate for constructing complex molecular structures. Its ability to undergo selective functional group transformations makes it a valuable tool for the creation of diverse chemical libraries and the development of new materials with tailored properties. Overall, the versatility and reactivity of 3-(Piperidin-1-yl)phenol make it an indispensable building block for chemists engaged in drug discovery, materials science, and agrochemical research.