(2S)-1-(4-methoxyphenyl)propan-2-amine hydrochloride

Base Information

Chemical Name:(2S)-1-(4-methoxyphenyl)propan-2-amine hydrochloride
CAS No.:50505-81-2
Molecular Formula:C₁₀H₁₅NO*ClH
Molecular Weight:201.696
Hs Code.:
UNII:W3WZ7STA2Y
Mol file:50505-81-2.mol

Synonyms:50505-81-2;(+)-p-Methoxyamphetamine hydrochloride;Pma hydrochloride, (S)-;W3WZ7STA2Y;4-Ma hydrochloride, (S)-;(2S)-1-(4-methoxyphenyl)propan-2-amine hydrochloride;D-p-Methoxyamphetamine hydrochloride;AKOS027340052;D-Para-methoxyamphetamine hydrochloride;Pma (psychedelic) hydrochloride, (S)-;4-Methoxyamphetamine hydrochloride, (S)-;(s)-(+)-4-methoxyamphetamine hydrochloride;Para-methoxyamphetamine hydrochloride, (S)-;F13082;(1S)-2-(4-Methoxyphenyl)-1-methylethylamine HCl;(S)-2-(4-Methoxyphenyl)-1-MethylethanaMine HCl;(S)-1-(4-METHOXYPHENYL)PROPAN-2-AMINE HCL;Benzeneethanamine, 4-methoxy-alpha-methyl-, hydrochloride, (S)-;Benzeneethanamine, 4-methoxy-alpha-methyl-, hydrochloride (1:1), (alphaS)-;Benzeneethanamine, 4-methoxy-alpha-methyl-, hydrochloride, (alphaS)-

Suppliers and Price of (2S)-1-(4-methoxyphenyl)propan-2-amine hydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 6 raw suppliers

Chemical Property of (2S)-1-(4-methoxyphenyl)propan-2-amine hydrochloride

Chemical Property:

Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:201.0920418
Heavy Atom Count:13
Complexity:119

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(CC1=CC=C(C=C1)OC)N.Cl
Isomeric SMILES:C[C@@H](CC1=CC=C(C=C1)OC)N.Cl

Technology Process of (2S)-1-(4-methoxyphenyl)propan-2-amine hydrochloride

There total 11 articles about (2S)-1-(4-methoxyphenyl)propan-2-amine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

: 122-84-9
4-methoxybenzyl methyl ketone

: 50505-81-2,52740-56-4
4-methoxyamphetamine

Guidance literature:: 4-methoxybenzyl methyl ketone; With ammonium hydroxide; hydrogen; at 50 ℃; for 20h; under 7500.75 Torr; Autoclave;

With hydrogenchloride; In diethyl ether;
DOI:10.1002/cssc.202100553

Reference yield: 89.0%

: C₁₅H₂₁NO₆S

: 50505-80-1,50505-81-2,52740-56-4
l-para-Methoxyamphetamine hydrochloride

Guidance literature:: C₁₅H₂₁NO₆S; With sodium tetrahydroborate; lithium chloride; In diethylene glycol dimethyl ether; at 80 ℃; for 24h;

With hydrogenchloride; In ethyl acetate; at 30 ℃; for 12h;

Reference yield: 86.0%

: 115424-09-4
N-Cbz-2-(4-methoxyphenyl)-1-methylethylamine

: 50505-80-1,50505-81-2,52740-56-4
l-para-Methoxyamphetamine hydrochloride

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; for 3h; Ambient temperature;
DOI:10.1080/00397919808007167