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639869

Sigma-Aldrich

4-Phenylpiperidine

97%

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1 G
657,00 kr
5 G
1 620,00 kr

657,00 kr

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1 G
657,00 kr
5 G
1 620,00 kr

About This Item

Empirical Formula (Hill Notation):
C11H15N
CAS Number:
771-99-3
Molecular Weight:
161.24
Beilstein:
124508
EC Number:
212-243-1
MDL number:
MFCD00006002
UNSPSC Code:
12352100
PubChem Substance ID:
24883062
NACRES:
NA.22

657,00 kr

Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

100

Assay

97%

mp

61-65 °C (lit.)

functional group

phenyl

SMILES string

C1CC(CCN1)c2ccccc2

InChI

1S/C11H15N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-5,11-12H,6-9H2

InChI key

UTBULQCHEUWJNV-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB1888
SDBB0722
SDBB0325
STBL3815
S32795

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Xing-hai Wang et al.
European journal of medicinal chemistry, 41(2), 226-232 (2006-01-13)
A nonlinear QSAR study was conducted on a series of 4-phenylpiperidine derivatives (4PPs) acting as mu opioid agonists by three-layer back-propagation neural network (NN) method. At first a variety of molecular descriptors were calculated and then selected with two-stage least
P Singh et al.
Journal of enzyme inhibition, 16(4), 331-338 (2002-03-28)
Two series of compounds were recently reported as novel alpha1a-selective adrenoceptor antagonists. In the first series, a dihydropyrimidone moiety is attached to a 4-phenyl piperidine containing side chain, while in the second, it is linked to a 4-substituted phenyl piperazine
Paul J Emmerson et al.
European journal of pharmacology, 494(2-3), 121-130 (2004-06-24)
Differences in the anorectic activity of morphinan (e.g., naltrexone) and 3,4-dimethyl-4-(3-hydroxyphenyl)piperidine (4PP) opioid receptor antagonists have been described. In an attempt to explain these differences, the influence of Na(+) on opioid binding affinity and functional activity of 4PP antagonists was
Karel Vervisch et al.
Organic & biomolecular chemistry, 10(16), 3308-3314 (2012-03-14)
Non-activated 2-(4-chloro-2-cyano-2-phenylbutyl)aziridines were used as building blocks for the stereoselective synthesis of novel cis-2-cyanomethyl-4-phenylpiperidines via a microwave-assisted aziridine to piperidine ring expansion followed by a radical-induced nitrile translocation through initial formation and subsequent cleavage of intermediate bicyclic iminyl radicals. Furthermore
Clandestine drug synthesis.
W H Soine
Medicinal research reviews, 6(1), 41-74 (1986-01-01)
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