2-(4-Methoxyphenyl)piperidine - CAS 63359-20-6

Catalog:	BB032116
Product Name:	2-(4-Methoxyphenyl)piperidine
CAS:	63359-20-6
Synonyms:	2-(4-methoxyphenyl)piperidine; 2-(4-methoxyphenyl)piperidine

Technical Data

Patents

Computed Properties

IUPAC Name:	2-(4-methoxyphenyl)piperidine
Description:	2-(4-Methoxyphenyl)piperidine (CAS# 63359-20-6) is a useful research chemical.
Molecular Weight:	191.27
Molecular Formula:	C12H17NO
Canonical SMILES:	COC1=CC=C(C=C1)C2CCCCN2
InChI:	InChI=1S/C12H17NO/c1-14-11-7-5-10(6-8-11)12-4-2-3-9-13-12/h5-8,12-13H,2-4,9H2,1H3
InChI Key:	PFEQGLKEECTHNQ-UHFFFAOYSA-N
LogP:	2.83860

Publication Number	Title	Priority Date
CN-112707857-A	Method for preparing piperidine compound by hydrogen transfer reduction of pyridine compound	20201229
CN-109715614-A	The 6 yuan of cyclammonium or lactams replaced with urea and phenyl	20160921
WO-2010138490-A1	Benzoxazepines as inhibitors of mtor and methods of their use and manufacture	20090526
WO-2010067233-A1	1,2,4 triazolo [4, 3 -a] [1,5] benzodiazepin-5 (6h) -ones as agonists of the cholecystokinin-1 receptor (cck-ir)	20081208
US-2006154917-A1	Substituted (heterocycloalkyl)methyl azole derivatives as c5a receptor modulators	20030703

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Related Functional Groups

Piperidines

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[2091522-65-3]
tert-butyl 3-cyano-5-hydroxypiperidine-1-carboxylate
[313685-03-9]
Ethyl 1-[(4-chlorophenyl)sulfonyl]piperidine-4-carboxylate
[1005629-22-0]
Ethyl 1-((1-ethyl-3-methyl-1H-pyrazol-4-yl)sulfonyl)piperidine-3-carboxylate
[681428-42-2]
Ethyl 1-(1-methylpyrazolo[3,4-d]pyrimidin-4-yl)piperidine-4-carboxylate

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Complexity:	164
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	191.131014166
Formal Charge:	0
Heavy Atom Count:	14
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	191.131014166
Rotatable Bond Count:	2
Topological Polar Surface Area:	21.3
Undefined Atom Stereocenter Count:	1
Undefined Bond Stereocenter Count:	0
XLogP3:	2.1