4-Nitro-3-acetamidocarbazole

Base Information

Chemical Name:4-Nitro-3-acetamidocarbazole
CAS No.:96014-34-5
Molecular Formula:C₁₄H₁₁N₃O₃
Molecular Weight:269.26
Hs Code.:
DSSTox Substance ID:DTXSID70242091
Wikidata:Q83125686

Synonyms:4-Nitro-3-acetamidocarbazole;CCRIS 7612;96014-34-5;DTXSID70242091

Suppliers and Price of 4-Nitro-3-acetamidocarbazole

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of 4-Nitro-3-acetamidocarbazole

Chemical Property:

Vapor Pressure:2E-14mmHg at 25°C
Boiling Point:601.5°C at 760 mmHg
Flash Point:317.6°C
PSA：94.20000
Density:1.488g/cm³
LogP:4.36040
XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:269.08004122
Heavy Atom Count:20
Complexity:409

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=C(C2=C(C=C1)NC3=CC=CC=C32)[N+](=O)[O-]

Technology Process of 4-Nitro-3-acetamidocarbazole

There total 3 articles about 4-Nitro-3-acetamidocarbazole 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: 56.0%

: 96014-33-4
acetylamino-3 benzoyl-9 nitro-4 carbazole

: 96014-34-5
3-Acetamido-4-nitro-9H-carbazole

Guidance literature:: With sodium hydroxide; In ethanol; at 80 ℃; for 0.166667h;

Reference yield:

: 96014-30-1
amino-3 benzoyl-9 carbazole

: 96014-34-5
3-Acetamido-4-nitro-9H-carbazole

Guidance literature:: Multi-step reaction with 3 steps

1: 64 percent / 1 h / Ambient temperature

2: 24 percent / HNO₃ / acetic acid / 2.5 h / Heating

3: 56 percent / 30percent NaOH / ethanol / 0.17 h / 80 °C

With sodium hydroxide; nitric acid; In ethanol; acetic acid;

Reference yield:

: 96014-31-2
acetylamino-3 benzoyl-9 carbazole

: 96014-34-5
3-Acetamido-4-nitro-9H-carbazole

Guidance literature:: Multi-step reaction with 2 steps

1: 24 percent / HNO₃ / acetic acid / 2.5 h / Heating

2: 56 percent / 30percent NaOH / ethanol / 0.17 h / 80 °C

With sodium hydroxide; nitric acid; In ethanol; acetic acid;