20388-87-8
- Product Name：2-Phenylpropan-1-amine hydrochloride
- Molecular Formula：C9H14ClN
- Purity：99%
- Molecular Weight：171.67
Product Details;
CasNo： 20388-87-8
Molecular Formula： C9H14ClN
Buy Reliable Quality 2-Phenylpropan-1-amine hydrochloride, Factory Sells 20388-87-8 with Cheap Price
- Molecular Formula:C9H14ClN
- Molecular Weight:171.67
- Vapor Pressure:0.197mmHg at 25°C
- Melting Point:143-144℃
- Boiling Point:210 °C at 760 mmHg
- Flash Point:84.6 °C
- PSA：26.02000
- LogP:3.25110
2-Phenylpropan-1-amine hydrochloride (Cas 20388-87-8) Usage
|
Description |
2-Phenylpropan-1-amine hydrochloride is a phenethylamine compound and positional isomer of amphetamine that has been found in nutritional supplements and classified as a novel doping substance. It acts as an agonist of the human trace amine-associated receptor 1 (EC50s = 325 and 104 nM for R(+) and S(-) isomers, respectively). |
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Uses |
2-phenyl-1-propylamine hydrochloride is an amine organic compound, which can be used as pharmaceutical intermediates. |
InChI:InChI=1/C9H13N.ClH/c1-8(7-10)9-5-3-2-4-6-9;/h2-6,8H,7,10H2,1H3;1H
20388-87-8 Relevant articles
Two-dimensional perovskite chiral ferromagnets
Li, Xiang-Yang,Liu, Xiao-Fei,Shao, Xiangfeng,Sun, Bing,Yang, Dezheng,Zhang, Hao-Li,Zhang, Yamin
, p. 8914 - 8920 (2020/12/09)
Magnetic molecular materials with a chir...
TRP-M8 RECEPTOR LIGANDS AND THEIR USE IN TREATMENTS
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Page/Page column 70, (2009/07/17)
Tetrahydroisoquinoline compounds of form...
AMPA RECEPTOR POTENTIATORS
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Page/Page column 6, (2008/12/06)
The present invention relates to a compo...
Synthesis of primary amines by the electrophilic amination of Grignard reagents with 1,3-dioxolan-2-one O-sulfonyloxime
Kitamura, Mitsuru,Suga, Takahiro,Chiba, Shunsuke,Narasaka, Koichi
, p. 4619 - 4621 (2007/10/03)
(Chemical equation presented) Primary am...
20388-87-8 Process route
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- 1823-91-2
1-phenylethyl cyanide
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- 20388-87-8,52991-03-4
rac-β-methylphenethylamine hydrochloride
| Conditions | Yield |
|---|---|
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With hydrogenchloride; hydrogen; 5%-palladium/activated carbon; In ethanol; water; at 50 - 64 ℃; for 3h; under 3878.71 - 4033.86 Torr;
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76.2% |
|
With hydrogenchloride; hydrogen; 5%-palladium/activated carbon; In ethanol; water; at 50 - 64 ℃; for 3h; under 3878.71 - 4033.86 Torr;
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76.2% |
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With hydrogenchloride; hydrogen; 5% palladium-on-charcoal; In ethanol; water; at 50 - 64 ℃; for 3h; under 3878.71 - 4033.86 Torr;
|
76.2% |
|
1-phenylethyl cyanide; With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; for 3.5h; Heating / reflux;
With sodium hydroxide; water; In diethyl ether; at 0 - 20 ℃; for 1.5h;
With hydrogenchloride; In diethyl ether;
|
-
- 1634-04-4
tert-butyl methyl ether
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- 1823-91-2
1-phenylethyl cyanide
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- 20388-87-8,52991-03-4
rac-β-methylphenethylamine hydrochloride
| Conditions | Yield |
|---|---|
|
With hydrogenchloride; palladium; In ethanol;
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76.2% |
|
With hydrogenchloride; palladium; In ethanol;
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76.2% |
20388-87-8 Upstream products
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31731-86-9
2-phenylpropylmagnesium bromide
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1823-91-2
1-phenylethyl cyanide
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1634-04-4
tert-butyl methyl ether
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582-22-9
2-phenylpropylamine
20388-87-8 Downstream products
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582-22-9
2-phenylpropylamine
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1016057-29-6
N-(2-phenylpropyl)-4-(trifluoromethyl)benzamide
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