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线性分子式:
ClC6H4CH2CH2NH2
化学文摘社编号:
分子量:
155.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-853-4
Beilstein/REAXYS Number:
508247
MDL number:
Assay:
98%
Form:
liquid
InChI
1S/C8H10ClN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2
InChI key
SRXFXCKTIGELTI-UHFFFAOYSA-N
SMILES string
NCCc1ccc(Cl)cc1
assay
98%
form
liquid
Quality Level
bp
60-65 °C/0.1 mmHg (lit.)
density
1.112 g/mL at 25 °C (lit.)
drug control
Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
222.8 °F - closed cup
flash_point_c
106 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
E Chung Hwang et al.
The Journal of pharmacology and experimental therapeutics, 213(2), 254-260 (1980-05-01)
A series of substituted phenylethylamines were examined for their relative potencies to 1) release and inhibit accumulation of labeled serotonin in brain synaptosomes, 2) compete with serotonin receptor binding and 3) induce the "serotonin syndrome" in mice. In general, the
T N Mellin et al.
The American journal of tropical medicine and hygiene, 32(1), 83-93 (1983-01-01)
Neuropharmacological studies of Schistosoma mansoni were conducted in vitro using visual observations of motor activity and measurements of worm length and extracellular electrical activity. The instrumentation and methodology described quantitatively measure extracellular electrical potentials associated with motor activity, and provide
Khalid Touiki et al.
Psychopharmacology, 182(4), 562-569 (2005-09-01)
Harmane and norharmane (two beta-carbolines) are tobacco components or products. The effects of harmane and norharmane on serotonergic raphe neurons remain unknown. Harmane and norharmane are inhibitors of the monoamine oxidases A (MAO-A) and B (MAO-B), respectively. To study the
Giulia Guiducci et al.
Nucleic acids research, 47(8), 4240-4254 (2019-02-28)
Enzymes of intermediary metabolism are often reported to have moonlighting functions as RNA-binding proteins and have regulatory roles beyond their primary activities. Human serine hydroxymethyltransferase (SHMT) is essential for the one-carbon metabolism, which sustains growth and proliferation in normal and
G B Baker et al.
Progress in neuro-psychopharmacology & biological psychiatry, 6(4-6), 343-346 (1982-01-01)
1. The accumulation of p-chlorophenylethylamine (pCPE) in rat brain after administration of pargyline plus p-chlorophenylalanine (pCPA) is demonstrated. 2. Measurements of pCPE in brain were performed at 0.25 h, 1 h and 4 h after administration of pCPA to pargyline-pretreated
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