Acetamide, 2-hydroxy-N-[4-(2-phenyldiazenyl)phenyl]-

Base Information

Chemical Name:Acetamide, 2-hydroxy-N-[4-(2-phenyldiazenyl)phenyl]-
CAS No.:87711-66-8
Molecular Formula:C₁₄H₁₃N₃O₂
Molecular Weight:255.276
Hs Code.:
DSSTox Substance ID:DTXSID401039161

Synonyms:Acetamide, 2-hydroxy-N-[4-(2-phenyldiazenyl)phenyl]-;DTXSID401039161;87711-66-8

Suppliers and Price of Acetamide, 2-hydroxy-N-[4-(2-phenyldiazenyl)phenyl]-

Supply Marketing:

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

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Chemical Property of Acetamide, 2-hydroxy-N-[4-(2-phenyldiazenyl)phenyl]-

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:255.100776666
Heavy Atom Count:19
Complexity:306

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)N=NC2=CC=C(C=C2)NC(=O)CO

Technology Process of Acetamide, 2-hydroxy-N-[4-(2-phenyldiazenyl)phenyl]-

There total 4 articles about Acetamide, 2-hydroxy-N-[4-(2-phenyldiazenyl)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: 32.0%

: 623-50-7
ethyl 2-hydroxyacetate

: 60-09-3
aniline yellow

: 87711-66-8
p-(hydroxyacetamido)azobenzene

Guidance literature:: In benzene; for 6h; Heating;
DOI:10.1021/jm00366a026

Reference yield:

: 60-09-3
aniline yellow

: 87711-66-8
p-(hydroxyacetamido)azobenzene

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / Na₂CO₃ / CHCl₃; H₂O

2: 3 h / 50 °C

3: 25percent NH₄OH / 0.5 h / Ambient temperature

With ammonium hydroxide; sodium carbonate; In chloroform; water;
DOI:10.1135/cccc19921495