1-Bromo-2-nitronaphthalene

Base Information

• Chemical Name: 1-Bromo-2-nitronaphthalene
• CAS No.: 4185-55-1
• Molecular Formula: C10H6BrNO2
• Molecular Weight: 252.067
• Hs Code.: 2904909090
• DSSTox Substance ID: DTXSID10409227
• Wikidata: Q82214963
• Mol file: 4185-55-1.mol

Synonyms:1-bromo-2-nitronaphthalene;4185-55-1;MFCD00971807;Nitrobromnaphtalin;1-Brom-2-nitronaphthalin;SCHEMBL9489459;DTXSID10409227;AKOS028114910;CS-12586;SY096837;CS-0161711;A854276

Chemical Property of 1-Bromo-2-nitronaphthalene

Chemical Property:

• Melting Point: 98-99 °C
• Boiling Point: 338.1±15.0 °C(Predicted)
• PSA: 45.82000
• Density: 1.662±0.06 g/cm3(Predicted)
• LogP: 4.03370
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 250.95819
• Heavy Atom Count: 14
• Complexity: 229

Purity/Quality:

98% ^*data from raw suppliers

1-Bromo-2-nitronaphthalene 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C=CC(=C2Br)[N+](=O)[O-]

Technology Process of 1-Bromo-2-nitronaphthalene

There total 5 articles about 1-Bromo-2-nitronaphthalene 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:

2-nitro-1-naphthylamine (607-23-8) → 1-bromo-2-nitro-naphthalene (4185-55-1)

Guidance literature:

Reference yield:

2-nitro-1-naphthol (607-24-9) → 1-bromo-2-nitro-naphthalene (4185-55-1)

Guidance literature:

Multi-step reaction with 2 steps

1: water; ammonium carbonate; ammonia / 120 - 130 °C

With ammonium carbonate; ammonia; water;

Reference yield:

5-bromo-6-nitro-1,2,3,4-tetrahydro-naphthalene → 1-bromo-2-nitro-naphthalene (4185-55-1)

Guidance literature:

With bromine;

upstream raw materials:

2-nitro-1-naphthylamine

8-Brom-naphthalinsulfonsaeure

bromine

2-nitro-1-naphthol

Downstream raw materials:

7H-dibenzo[c,g]carbazole

2-nitro-1-phenylnaphthalene

benzo[c]carbazole