73659
1-(4-氯苯基)哌嗪
≥98.0% (GC)
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关于此项目
经验公式（希尔记法）:
C10H13ClN2
化学文摘社编号:
分子量:
196.68
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
150981
Assay:
≥98.0% (GC)
Form:
crystals
InChI
1S/C10H13ClN2/c11-9-1-3-10(4-2-9)13-7-5-12-6-8-13/h1-4,12H,5-8H2
SMILES string
Clc1ccc(cc1)N2CCNCC2
InChI key
UNEIHNMKASENIG-UHFFFAOYSA-N
assay
≥98.0% (GC)
form
crystals
drug control
Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet
mp
76-79 °C
functional group
chloro
Quality Level
Gene Information
rat ... Htr3a(79246)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
R W Fuller et al.
Research communications in chemical pathology and pharmacology, 29(1), 201-204 (1980-07-01)
1-(p-Chlorophenyl)piperazine (PCPP), a structural analog of p-chloroamphetamine (PCA), increased serotonin and decreased 5-hydroxyindoleacetic acid (5-HIAA) concentration in rat brain at 6 hours. At one day and one week, serotonin and 5-HIAA concentrations were normal. In contrast, PCA lowered serotonin and
J Maj et al.
Polish journal of pharmacology and pharmacy, 32(4), 495-504 (1980-07-01)
Studies of 1-(m-chlorophenyl)-piperazine (m-CPP), 1-(p-chlorophenyl)-piperazine (p-CPP) and 1-phenylpiperazine (PP) were carried out on rats, mice and rabbits in order to assess their stimulatory effect on the central serotonin system. It was found out that m-CPP and p-CPP evoked a characteristic
Piotr Cysewski
Journal of molecular modeling, 23(4), 136-136 (2017-03-30)
In silico screening was performed to search for binary solids in which a phenylpiperazine-derivative drug was cocrystallized with a dicarboxylic acid. The phenylpiperazine derivative could be any of 61 such drugs, while the dicarboxylic acid could be any of nine
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