Etilamfetamine

Base Information

• Chemical Name: Etilamfetamine
• CAS No.: 457-87-4
• Molecular Formula: C11H17 N
• Molecular Weight: 163.263
• European Community (EC) Number: 803-956-4
• UNII: 022YON1XMX
• DSSTox Substance ID: DTXSID10860359
• Nikkaji Number: J5.759B
• Wikipedia: Etilamfetamine
• Wikidata: Q5404591
• NCI Thesaurus Code: C81050
• Metabolomics Workbench ID: 154110
• ChEMBL ID: CHEMBL276443
• Mol file: 457-87-4.mol

Synonyms:ethylamphetamine;ethylamphetamine hydrochloride;ethylamphetamine hydrochloride, (+-)-isomer;ethylamphetamine hydrochloride, (R)-isomer;ethylamphetamine, (R)-isomer;N-ethylamphetamine

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

Chemical Property of Etilamfetamine

Chemical Property:

• Vapor Pressure: 0.0503mmHg at 25°C
• Refractive Index: nD25 1.4986
• Boiling Point: 235.3°Cat760mmHg
• PKA: pKa 10.23 (Uncertain)
• Flash Point: 95.5°C
• PSA: 12.03000
• Density: 0.902g/cm³
• LogP: 2.61800
• Storage Temp.: 2-8°C
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 163.136099547
• Heavy Atom Count: 12
• Complexity: 106

Purity/Quality:

Safty Information:

• Pictogram(s): F,T
• Hazard Codes: F,T
• Statements: 11-23/24/25-39/23/24/25
• Safety Statements: 7-16-36/37-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCNC(C)CC1=CC=CC=C1

Technology Process of Etilamfetamine

There total 10 articles about Etilamfetamine 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: 64.0%

(2-nitroprop-1-enyl)benzene (705-60-2) + lithium triethylborohydride (22560-16-3) → N-ethylamphetamine (457-87-4)

Guidance literature:

With borane-THF; In tetrahydrofuran; at 60 - 70 ℃; for 15h; other conjugated nitroalkenes;

DOI:10.1016/S0040-4020(01)89059-1

Reference yield:

phenyldiazomethane (908094-04-2) + diethylamine (109-89-7) → stilbene (588-59-0) + N,N-diethylbenzylamine (772-54-3) + N-ethylamphetamine (457-87-4) + 1,1'-(1,2-ethanediyl)bisbenzene (103-29-7) + toluene (108-88-3,15644-74-3,16713-13-6)

Guidance literature:

Product distribution; Irradiation;

Reference yield:

N-ethyl-N-methylamphetamine (119290-77-6) → methamphetamin (7632-10-2) + N-ethylamphetamine (457-87-4)

Guidance literature:

Rate constant;

DOI:10.1002/jps.2600690505

upstream raw materials:

ethylamine

1-phenyl-acetone

N-formylethylamine

phenyldiazomethane

Downstream raw materials:

ethyl-heptyl-(1-methyl-2-phenyl-ethyl)-amine

N-Ethyl-N-( 1-methyl-phenethyl )-bernsteinsaeure-ethylester-amid

ethyl-(1-methyl-2-phenyl-ethyl)-(7-nitro-benzo[1,2,5]oxadiazol-4-yl)-amine

2-amino-1-phenylpropane

Refernces

• 1、 -. "Derivatives, immunogens, and antibodies for detecting ecstasy-class drugs". . . Retrieved 2008/06/13.
• 2、 -. "Derivatives of amphetamine, antibodies against said derivatives, reagent kits, methods of producing said antibodies, and methods of detecting said derivatives". . . Retrieved 2008/06/13.