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Merck

C4265

Sigma-Aldrich

2-(4-氯苯基)丙-1-胺 盐酸盐

≥98%

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About This Item

经验公式(希尔记法):
C9H12ClN · HCl
CAS号:
分子量:
206.11
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

≥98%

形狀

powder

儲存溫度

2-8°C

SMILES 字串

Cl[H].CC(CN)c1ccc(Cl)cc1

InChI

1S/C9H12ClN.ClH/c1-7(6-11)8-2-4-9(10)5-3-8;/h2-5,7H,6,11H2,1H3;1H

InChI 密鑰

RTPMRVSAKBTCBG-UHFFFAOYSA-N

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象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析证书(COA)

Lot/Batch Number

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H Kinemuchi et al.
Japanese journal of pharmacology, 46(2), 197-199 (1988-02-01)
To further clarify highly MAO-A- or -B-selective inhibitory properties of 5-fluoro-alpha-methyltryptamine (5-FMT) and p-chloro-beta-methylphenethylamine (p-CMPEA), we determined the types and K1 values of inhibition of rat brain MAO-A and -B activity in vitro. The kinetic data obtained showed that 5-FMT
S K Kim et al.
Neuropharmacology, 30(4), 329-335 (1991-04-01)
Various intraperitoneal doses of 5-fluoro-alpha-methyltryptamine (5-FMT), given to mice, dose-dependently inhibited only MAOA activity, with similar degrees of inhibition in the striatum, hypothalamus and the rest of the forebrain. The activity inhibited in these regions, completely recovered to control levels
H Kinemuchi et al.
Research communications in chemical pathology and pharmacology, 54(1), 125-128 (1986-10-01)
In order to develop new and potent reversible MAO-B-selective inhibitors, we examined the inhibitory effects of two substrate-analogues, 5-fluoro-alpha-methyltryptamine (5-FMT) and p-chloro-beta-methylphenethylamine (p-CMP) on rat brain MAO-A and -B activity in vitro. Studies of the inhibitory effects of both analogues

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