N,N-Diphenylethylenediamine

Base Information

• Chemical Name: N,N-Diphenylethylenediamine
• CAS No.: 1140-29-0
• Molecular Formula: C14H16N2
• Molecular Weight: 212.294
• Hs Code.: 2921590090
• DSSTox Substance ID: DTXSID40529548
• Nikkaji Number: J1.137.254F
• Wikidata: Q82400032
• Mol file: 1140-29-0.mol

Synonyms:N,N-DIPHENYLETHYLENEDIAMINE;1140-29-0;N',N'-diphenylethane-1,2-diamine;N1,N1-DIPHENYLETHANE-1,2-DIAMINE;n,n-diphenylethane-1,2-diamine;starbld0004515;SCHEMBL150157;N-(2-aminoethyl)-diphenylamine;DTXSID40529548;PADPKJACPLYMPK-UHFFFAOYSA-N;N~1~,N~1~-Diphenylethane-1,2-diamine;A809058

Chemical Property of N,N-Diphenylethylenediamine

Chemical Property:

• PSA: 29.26000
• LogP: 3.48370
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 212.131348519
• Heavy Atom Count: 16
• Complexity: 163

Purity/Quality:

98%,99%, ^*data from raw suppliers

N,N′-Diphenylethylenediamine 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)N(CCN)C2=CC=CC=C2

Technology Process of N,N-Diphenylethylenediamine

There total 13 articles about N,N-Diphenylethylenediamine 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: 78.0%

C15H17N3O (1333418-02-2) → N-(2-aminoethyl)-N-phenylaniline (1140-29-0)

Guidance literature:

With hydrogenchloride; sodium nitrate; In water; at 0 - 80 ℃; for 7h;

Reference yield: 76.0%

2-<2-(diphenylamino)ethyl>-1H-isoindole-1,3(2H)-dione (86922-38-5) → N-(2-aminoethyl)-N-phenylaniline (1140-29-0)

Guidance literature:

With hydrazine hydrate; In ethanol; for 3h; Heating;

DOI:10.1021/jm00365a016

Reference yield:

ethanol (64-17-5) + (1E,2E)-1,2-diphenylethane-1,2-dione bis(phenylhydrazone) (572-18-9) → N-(2-aminoethyl)-N-phenylaniline (1140-29-0) + 2,3,5,6-tetraphenylpyrazine (642-04-6) + erythro-2-amino-1,2-diphenylethanol (530-36-9,3764-63-4,13286-63-0,23190-16-1,23190-17-2,23364-44-5,23412-95-5,39664-87-4,88082-66-0)

Guidance literature:

upstream raw materials:

2-<2-(diphenylamino)ethyl>-1H-isoindole-1,3(2H)-dione

4,5-diphenyl-2,5-dihydro-1H-imidazol-2-ol

hydrogen bromide

acetic acid

Downstream raw materials:

Diphenylacetaldehyde

1,2-diphenyl-1,2-ethanediol

threo-1,2-diphenyl-2-aminoethan-1-ol

isoamarine