4'-((p-(Dimethylamino)phenyl)azo)acetanilide

Base Information

• Chemical Name: 4'-((p-(Dimethylamino)phenyl)azo)acetanilide
• CAS No.: 1591-56-6
• Molecular Formula: C16H18 N4 O
• Molecular Weight: 282.345
• Hs Code.: 2927000090
• DSSTox Substance ID: DTXSID001030836
• Nikkaji Number: J519.297H
• Mol file: 1591-56-6.mol

Synonyms:4'-((p-(Dimethylamino)phenyl)azo)acetanilide;N'-Acadab;1591-56-6;CCRIS 2254;BRN 0755016;C.I. 11030;N'-Acetyl-4'-amino-N,N-dimethyl-4-aminoazobenzene;N-(4-((4-(Dimethylamino)phenyl)azo)phenyl)acetamide;Acetamide, N-(4-((4-(dimethylamino)phenyl)azo)phenyl)-;N-[4-[[4-(dimethylamino)phenyl]diazenyl]phenyl]acetamide;4-16-00-00517 (Beilstein Handbook Reference);C16H18N4O;ACETANILIDE, 4'-((P-(DIMETHYLAMINO)PHENYL)AZO)-;Acetanilide, 4'-[[p-(dimethylamino)phenyl]azo]-;Acetamide, N-[4-[[4-(dimethylamino)phenyl]azo]phenyl]-;N-[4-[[4-(DIMETHYLAMINO)PHENYL]AZO]PHENYL]ACETAMIDE;SCHEMBL8817969;SCHEMBL12125125;DTXSID001030836;LS-9327;4/'-((p-(Dimethylamino)phenyl)azo)acetanilide;N,N-Dimethyl-N'-acetylazobenzene-4,4'-diamine

Chemical Property of 4'-((p-(Dimethylamino)phenyl)azo)acetanilide

Chemical Property:

• Vapor Pressure: 5.1E-11mmHg at 25°C
• Boiling Point: 522.6°C at 760 mmHg
• Flash Point: 269.9°C
• PSA: 60.55000
• Density: 1.11g/cm³
• LogP: 4.77590
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 282.14806121
• Heavy Atom Count: 21
• Complexity: 353

Purity/Quality:

99%min ^*data from raw suppliers

4'-((P-(DIMETHYLAMINO)PHENYL)AZO)ACETANILIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1=CC=C(C=C1)N=NC2=CC=C(C=C2)N(C)C

Technology Process of 4'-((p-(Dimethylamino)phenyl)azo)acetanilide

There total 5 articles about 4'-((p-(Dimethylamino)phenyl)azo)acetanilide 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:

4-nitrobenzenediazonium chloride (100-05-0) → acetic acid-[4-(4-dimethylamino-phenylazo)-anilide] (1591-56-6)

Guidance literature:

Multi-step reaction with 3 steps

1: water

2: alcohol; ammonium sulfide

With ammonium sulfide; ethanol; water;

Reference yield:

N,N-dimethyl-4-(4-nitrophenylazo)aniline (2491-74-9,55252-43-2,73815-07-3) → acetic acid-[4-(4-dimethylamino-phenylazo)-anilide] (1591-56-6)

Guidance literature:

Multi-step reaction with 2 steps

1: alcohol; ammonium sulfide

With ammonium sulfide; ethanol;

Reference yield:

N,N-dimethyl-aniline (121-69-7,77733-26-7) → acetic acid-[4-(4-dimethylamino-phenylazo)-anilide] (1591-56-6)

Guidance literature:

upstream raw materials:

acetic anhydride

N,N-dimethyl-4,4'-azodianiline

N,N-dimethyl-aniline

4-nitrobenzenediazonium chloride

Downstream raw materials:

N,N-dimethyl-4,4'-azodianiline

chloro-acetic acid-[4-(4-dimethylamino-phenylazo)-anilide]