3-(2-Aminoanilino)propanenitrile

Base Information

Chemical Name:3-(2-Aminoanilino)propanenitrile
CAS No.:98997-02-5
Molecular Formula:C9H11N3
Molecular Weight:161.206
Hs Code.:
DSSTox Substance ID:DTXSID80565824
Wikidata:Q82451113

Synonyms:98997-02-5;3-[(2-AMINOPHENYL)AMINO]PROPANENITRILE;3-(2-Aminoanilino)propanenitrile;SCHEMBL23908718;DTXSID80565824;G45688;EN300-7854088

Suppliers and Price of 3-(2-Aminoanilino)propanenitrile

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-(2-Aminoanilino)propanenitrile

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:161.095297364
Heavy Atom Count:12
Complexity:170

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)N)NCCC#N

Technology Process of 3-(2-Aminoanilino)propanenitrile

There total 3 articles about 3-(2-Aminoanilino)propanenitrile 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: 82.0%

: 107-13-1,25014-41-9
acrylonitrile

: 95-54-5
1,2-diamino-benzene

: 98997-02-5
3-(2-aminophenylamino)propanenitrile

Guidance literature:: With MCM-41 immobilized phenanthrolinium dibromide; In water; at 20 ℃; for 1.5h; Catalytic behavior;
DOI:10.1007/s10562-016-1743-4

Reference yield:

: 88-74-4
2-nitro-aniline

: 98997-02-5
3-(2-aminophenylamino)propanenitrile

Guidance literature:: Multi-step reaction with 2 steps

1: Triton B / dioxane

2: H₂ / Pd/C

With hydrogen; N-benzyl-trimethylammonium hydroxide; palladium on activated charcoal; In 1,4-dioxane;
DOI:10.1021/jm00001a005