(+)-p-Chloroamphetamine hydrochloride

Base Information

• Chemical Name: (+)-p-Chloroamphetamine hydrochloride
• CAS No.: 16064-30-5
• Molecular Formula: C₉H₁₂ClN*ClH
• Molecular Weight: 206.115
• UNII: BGE5V6Y2ZA
• DSSTox Substance ID: DTXSID50936360

Synonyms:16064-30-5;(+)-p-Chloroamphetamine hydrochloride;BGE5V6Y2ZA;(1S)-2-(4-CHLOROPHENYL)-1-METHYLETHYLAMINE HYDROCHLORIDE;p-Chloroamphetamine hydrochloride, (S)-;(1s)-2-(4-chlorophenyl)-1-methylethylamine hcl;(+)-p-Chloro-alpha-methylphenethylamine hydrochloride;(2S)-1-(4-chlorophenyl)propan-2-amine;hydrochloride;Phenethylamine, p-chloro-alpha-methyl-, hydrochloride, (+)-;UNII-BGE5V6Y2ZA;SCHEMBL3279916;DTXSID50936360;AKOS037644306;AS-49849;LS-103241;N11302;(S)-(+)-P-CHLOROAMPHETAMINE HYDROCHLORIDE;1-(4-Chlorophenyl)propan-2-amine--hydrogen chloride (1/1);BENZENEETHANAMINE, 4-CHLORO-.ALPHA.-METHYL-, HYDROCHLORIDE, (S)-;PHENETHYLAMINE, P-CHLORO-.ALPHA.-METHYL-, HYDROCHLORIDE, (+)-;BENZENEETHANAMINE, 4-CHLORO-.ALPHA.-METHYL-, HYDROCHLORIDE (1:1), (.ALPHA.S)-

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of (+)-p-Chloroamphetamine hydrochloride

Chemical Property:

• Vapor Pressure: 0.0307mmHg at 25°C
• Boiling Point: 244.2°Cat760mmHg
• Flash Point: 117°C
• Density: g/cm³
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 205.0425048
• Heavy Atom Count: 12
• Complexity: 108

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of (+)-p-Chloroamphetamine hydrochloride

There total 1 articles about (+)-p-Chloroamphetamine 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:

p-chloroamphetamine hydrochloride (3706-38-5,25356-95-0) → (S)-α-(p-chlorobenzyl)ethylamine hydrochloride (16064-30-5,25356-95-0) + (R)-2-amino-1-(p-chlorophenyl)propane hydrochloride (25356-95-0)

Guidance literature:

With chiral stationary phase including isopropyl-functionalized CF₆; In methanol; acetic acid; triethylamine; acetonitrile; at 20 ℃; Purification / work up;

upstream raw materials:

p-chloroamphetamine hydrochloride