추천 제품
Quality Level
분석
≥97.0%
refractive index
n20/D 1.588 (lit.)
bp
286 °C (lit.)
density
1.062 g/mL at 25 °C (lit.)
SMILES string
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
InChI key
YZTJYBJCZXZGCT-UHFFFAOYSA-N
유전자 정보
mouse ... Htr3a(15561)
rat ... Drd2(24318) , Htr1a(24473)
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신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
284.0 °F
Flash Point (°C)
140 °C
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Gürkan Keşan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 88, 144-155 (2012-01-10)
New metal halide complexes in the form of M(pp)(2)Cl(2) (where pp=1-phenylpiperazine and M=Pd or Hg) have been prepared for the first time and their FT-IR and FT-Raman spectra are reported in the region of 4000-10 cm(-1) and 4000-50 cm(-1), respectively.
Jadwiga Handzlik et al.
Bioorganic & medicinal chemistry, 16(11), 5982-5998 (2008-05-21)
In the search for new antiarrhythmic agents, some active 2-methoxyphenylpiperazine derivatives of phenytoin were obtained as a chemical modification of compound AZ-99 (3-ethyl-1-[2-hydroxy-3-(4-phenylpiperazin-1-yl)-propyl]-2,4-dioxo-5,5-diphenylimidazolidine). These compounds possessed structural properties similar to those of alpha(1)-adrenoceptor antagonists. In the present study, the affinities
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
Jadwiga Handzlik et al.
Bioorganic & medicinal chemistry letters, 20(20), 6152-6156 (2010-09-04)
A series of phenylpiperazine derivatives of phenytoin was evaluated for their affinity at α(1)-adrenoceptor subtypes in functional bioassays (rat tail artery: α(1A) and/or α(1B); guinea pig spleen: α(1B); rat aorta: α(1D)). The most potent compounds at α(1A)-, α(1B)- and α(1D)-adrenoceptors
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