Diazenecarboximidamide, N-[(phenoxycarbonyl)oxy]-2-phenyl-

Base Information

Chemical Name:Diazenecarboximidamide, N-[(phenoxycarbonyl)oxy]-2-phenyl-
CAS No.:203793-57-1
Molecular Formula:C₁₄H₁₂N₄O₃
Molecular Weight:284.274
Hs Code.:
DSSTox Substance ID:DTXSID401191967

Synonyms:DTXSID401191967;Diazenecarboximidamide, N-[(phenoxycarbonyl)oxy]-2-phenyl-;203793-57-1

Suppliers and Price of Diazenecarboximidamide, N-[(phenoxycarbonyl)oxy]-2-phenyl-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Diazenecarboximidamide, N-[(phenoxycarbonyl)oxy]-2-phenyl-

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:284.09094026
Heavy Atom Count:21
Complexity:386

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)N=NC(=NOC(=O)OC2=CC=CC=C2)N
Isomeric SMILES:C1=CC=C(C=C1)N=N/C(=N/OC(=O)OC2=CC=CC=C2)/N

Technology Process of Diazenecarboximidamide, N-[(phenoxycarbonyl)oxy]-2-phenyl-

There total 3 articles about Diazenecarboximidamide, N-[(phenoxycarbonyl)oxy]-2-phenyl- 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: 34.0%

: 1885-14-9
phenyl chloroformate

: 52512-46-6
phenylazomethanamidoxime

: 203793-57-1
O-(phenoxycarbonyl)-phenylazo-methanamidoxime

Guidance literature:: With triethylamine; In diethyl ether; for 0.5h;
DOI:10.1002/ardp.19973301207

Reference yield:

: 62-53-3
aniline

: 203793-57-1
O-(phenoxycarbonyl)-phenylazo-methanamidoxime

Guidance literature:: Multi-step reaction with 3 steps

1: 1) 10percent aq. HCl, NaNO₂ / 1) 0 deg C to 5 deg C, 2) ether, 30 min

2: NH₂OH*HCl, NaOH / diethyl ether; H₂O

3: 34 percent / NEt₃ / diethyl ether / 0.5 h

With hydrogenchloride; sodium hydroxide; hydroxylamine hydrochloride; triethylamine; sodium nitrite; In diethyl ether; water;
DOI:10.1002/ardp.19973301207

Reference yield:

: 622-83-3
phenyl-diazenecarbonitrile

: 203793-57-1
O-(phenoxycarbonyl)-phenylazo-methanamidoxime

Guidance literature:: Multi-step reaction with 2 steps

1: NH₂OH*HCl, NaOH / diethyl ether; H₂O

2: 34 percent / NEt₃ / diethyl ether / 0.5 h

With sodium hydroxide; hydroxylamine hydrochloride; triethylamine; In diethyl ether; water;
DOI:10.1002/ardp.19973301207