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P30004

Sigma-Aldrich

1-Phenylpiperazine

≥97.0%

Sinônimo(s):

N-Phenyldiethylenediamine

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About This Item

Fórmula empírica (Notação de Hill):
C10H14N2
Número CAS:
92-54-6
Peso molecular:
162.23
Beilstein:
132157
Número CE:
202-165-6
Número MDL:
MFCD00005957
Código UNSPSC:
12352100
ID de substância PubChem:
24898377
NACRES:
NA.22

Ensaio

≥97.0%

índice de refração

n20/D 1.588 (lit.)

pb

286 °C (lit.)

densidade

1.062 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

C1CN(CCN1)c2ccccc2

InChI

1S/C10H14N2/c1-2-4-10(5-3-1)12-8-6-11-7-9-12/h1-5,11H,6-9H2

chave InChI

YZTJYBJCZXZGCT-UHFFFAOYSA-N

Informações sobre genes

mouse ... Htr3a(15561)
rat ... Drd2(24318) , Htr1a(24473)

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Pictogramas

Skull and crossbonesCorrosion
GHS06,GHS05

Palavra indicadora

Danger

Frases de perigo

H301,H310,H314

Classificações de perigo

Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

Código de classe de armazenamento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

284.0 °F

Ponto de fulgor (°C)

140 °C

Equipamento de proteção individual

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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4-Benzylpiperidine 99%

Sigma-Aldrich

142360

4-Benzylpiperidine

T H C Cheung et al.
Neuropharmacology, 63(8), 1346-1359 (2012-09-11)
This study examined cocaine self-administration after pretreatments with three structurally related compounds that bind selectively to dopamine D3 receptors (D3Rs) relative to the D2 receptor subtype (D2Rs) and exhibit varying intrinsic activities in the forskolin-stimulated adenylyl cyclase assay. The compounds
Justyna Fraczyk et al.
Journal of combinatorial chemistry, 11(3), 446-451 (2009-04-17)
A library of artificial receptors formed by the self-organization of N-lipidated peptides attached to cellulose via m-aminophenylamino-1,3,5-triazine was used for docking pairs of small colorless N-phenylpiperazines with and without a fluorine atom in the phenyl ring. The interactions of guests
Tiantian Mou et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 67(11), 2013-2018 (2009-08-15)
This study reports the synthesis and characterization of N-(3-(4-(2-methoxyphenyl)piperazin-1-yl)propyl-4-[(18)F]fluorobenzamide ([(18)F]MPP3F). The total reaction time for [(18)F]MPP3F, including final high-performance liquid chromatography purification, was about 3h. Typical decay-corrected radiochemical yield was 18.4+/-3.1%. The radiochemical purity was >98%. Biodistribution in mice showed
Romano Di Fabio et al.
Journal of medicinal chemistry, 52(10), 3238-3247 (2009-04-25)
In an effort to discover novel druglike NK(1) receptor antagonists a new series of suitably substituted C-phenylpiperazine derivatives was identified by an appropriate chemical exploration of related N-phenylpiperazine analogues, with the specific aim to maximize their in vitro affinity and
Jadwiga Handzlik et al.
Bioorganic & medicinal chemistry, 20(7), 2290-2303 (2012-03-03)
An association between α(1)-adrenoceptor affinities, hERG K(+)-antagonistic properties and antiarrhythmic activities for a series of phenylpiperazine derivatives of hydantoin (2a-21a) was investigated. New compounds were synthesized and tested for their affinity for α(1)-adrenoceptors in radioligand binding assay using [(3)H]-prazosin as
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