N-Isopropyl-alpha-(m-methylbenzyl)-2-thenylamine hydrochloride

Base Information

Chemical Name:N-Isopropyl-alpha-(m-methylbenzyl)-2-thenylamine hydrochloride
CAS No.:80154-85-4
Molecular Formula:C₁₆H₂₁NS*ClH
Molecular Weight:295.876
Hs Code.:
DSSTox Substance ID:DTXSID301001028
Mol file:80154-85-4.mol

Synonyms:N-Isopropyl-alpha-(m-methylbenzyl)-2-thenylamine hydrochloride;80154-85-4;2-Thenylamine, N-isopropyl-alpha-(m-methylbenzyl)-, hydrochloride;DTXSID301001028;LS-149342;N-[2-(3-Methylphenyl)-1-(thiophen-2-yl)ethyl]propan-2-amine--hydrogen chloride (1/1)

Suppliers and Price of N-Isopropyl-alpha-(m-methylbenzyl)-2-thenylamine 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 4 raw suppliers

Chemical Property of N-Isopropyl-alpha-(m-methylbenzyl)-2-thenylamine hydrochloride

Chemical Property:

Vapor Pressure:4.56E-05mmHg at 25°C
Boiling Point:349.9°C at 760 mmHg
Flash Point:165.4°C
PSA：40.27000
LogP:5.53120
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:295.1161486
Heavy Atom Count:19
Complexity:241

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC=C1)CC(C2=CC=CS2)NC(C)C.Cl

Technology Process of N-Isopropyl-alpha-(m-methylbenzyl)-2-thenylamine hydrochloride

There total 2 articles about N-Isopropyl-alpha-(m-methylbenzyl)-2-thenylamine 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:

: 1-Thiophen-2-yl-2-m-tolyl-ethanone

: 80154-85-4
Isopropyl-(1-thiophen-2-yl-2-m-tolyl-ethyl)-amine; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / (NH₄)2CO₃, HCOOH

2: 2.) NaBH₄ / 1.) 2.5 h, reflux, 2.) MeOH

With sodium tetrahydroborate; formic acid; ammonium carbonate;