1,2-Ethanediamine, 1,2-bis(4-methylphenyl)-

Base Information

Chemical Name:1,2-Ethanediamine, 1,2-bis(4-methylphenyl)-
CAS No.:124842-96-2
Molecular Formula:C16H20N2
Molecular Weight:240.348
Hs Code.:2921599090
Mol file:124842-96-2.mol

Synonyms:.meso-1,2-bis-(4-Methylphenyl)ethane-1,2-diamine;.1,2-Bis(4'-methylphenyl)ethan-1,2-diamin;dl-1,2-bis(4-methylphenyl)ethylenediamine;.meso-1,2-Bis-(4-methylphenyl)-aethylendiamin;

Suppliers and Price of 1,2-Ethanediamine, 1,2-bis(4-methylphenyl)-

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

SynQuest Laboratories
1,2-Di-p-tolylethylenediamine
1 g
$ 336.00

Crysdot
1,2-Di-p-tolylethylenediamine 95+%
5g
$ 422.00

Alichem
1,2-Di-p-tolylethylenediamine
5g
$ 468.60

Total 5 raw suppliers

Chemical Property of 1,2-Ethanediamine, 1,2-bis(4-methylphenyl)-

Chemical Property:

PSA：52.04000
LogP:4.40380

Purity/Quality:

97% ^*data from raw suppliers

1,2-Di-p-tolylethylenediamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,2-Ethanediamine, 1,2-bis(4-methylphenyl)-

There total 7 articles about 1,2-Ethanediamine, 1,2-bis(4-methylphenyl)- 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: 80.0%

: 104-87-0
4-methyl-benzaldehyde

: 124842-96-2
meso-1,2-bis(4-methylphenyl)ethylenediamine

Guidance literature:: With tris(bipyridine)ruthenium(II) dichloride hexahydrate; ammonia; N-ethyl-N,N-diisopropylamine; scandium tris(trifluoromethanesulfonate); In methanol; acetonitrile; at 0 - 25 ℃; for 15h; chemoselective reaction; Sealed tube; Inert atmosphere; Irradiation;
DOI:10.1021/acs.orglett.8b01637