N1-(2-Aminobenzyl)-1,2-benzenediamine

Base Information

Chemical Name:N1-(2-Aminobenzyl)-1,2-benzenediamine
CAS No.:14573-33-2
Molecular Formula:C13H15N3
Molecular Weight:213.282
Hs Code.:2921590090
DSSTox Substance ID:DTXSID00533186
Wikidata:Q82406329
Mol file:14573-33-2.mol

Synonyms:14573-33-2;N1-(2-Aminobenzyl)-1,2-benzenediamine;N1-(2-Aminobenzyl)benzene-1,2-diamine;2-N-[(2-aminophenyl)methyl]benzene-1,2-diamine;1,2-Benzenediamine, N1-[(2-aminophenyl)methyl]-;DTXSID00533186;MFCD14584822;AKOS005071758;AE-0726;SB78890;N1-[(2-aminophenyl)methyl]benzene-1,2-diamine;J-523364;N~1~-[(2-Aminophenyl)methyl]benzene-1,2-diamine

Suppliers and Price of N1-(2-Aminobenzyl)-1,2-benzenediamine

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

Matrix Scientific
N1-(2-Aminobenzyl)-1,2-benzenediamine >95%
1g
$ 454.00

Matrix Scientific
N1-(2-Aminobenzyl)-1,2-benzenediamine >95%
500mg
$ 362.00

Crysdot
N1-(2-Aminobenzyl)benzene-1,2-diamine 95+%
5g
$ 844.00

AK Scientific
N1-(2-Aminobenzyl)-1,2-benzenediamine
1g
$ 662.00

Total 6 raw suppliers

Chemical Property of N1-(2-Aminobenzyl)-1,2-benzenediamine

Chemical Property:

Melting Point:98～100℃
PSA：64.07000
LogP:3.69850
XLogP3:2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:213.126597491
Heavy Atom Count:16
Complexity:207

Purity/Quality:

98%min ^*data from raw suppliers

N1-(2-Aminobenzyl)-1,2-benzenediamine >95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)CNC2=CC=CC=C2N)N

Technology Process of N1-(2-Aminobenzyl)-1,2-benzenediamine

There total 4 articles about N1-(2-Aminobenzyl)-1,2-benzenediamine 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:

: 91532-59-1
o-nitrobenzo-1-nitro-2-naftalide

: 14573-33-2
N-<2-aminobenzil>-o-fenilendiamina

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / hydrogen / 10percent Pd/C / ethyl acetate / 4 h / Ambient temperature

2: LiAlH₄ / tetrahydrofuran / 8 h / Heating

With lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;

Reference yield:

: 610-14-0
2-nitrobenzyl chloride

: 14573-33-2
N-<2-aminobenzil>-o-fenilendiamina

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / triethylamine / dioxane / 3 h / Heating

2: 77 percent / hydrogen / 10percent Pd/C / ethyl acetate / 4 h / Ambient temperature

3: LiAlH₄ / tetrahydrofuran / 8 h / Heating

With lithium aluminium tetrahydride; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethyl acetate;