5-Amino-2-bromo-4-nitrophenol

Base Information

Chemical Name:5-Amino-2-bromo-4-nitrophenol
CAS No.:855836-08-7
Molecular Formula:C6H5BrN2O3
Molecular Weight:233.021
Hs Code.:2922299090
European Community (EC) Number:881-412-5
DSSTox Substance ID:DTXSID80681477
Wikidata:Q82605533
Mol file:855836-08-7.mol

Synonyms:5-AMINO-2-BROMO-4-NITROPHENOL;855836-08-7;DTXSID80681477;MFCD16036100;SB80720;BS-23321;A863535

Suppliers and Price of 5-Amino-2-bromo-4-nitrophenol

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

Crysdot
5-Amino-2-bromo-4-nitrophenol 95+%
25g
$ 677.00

Crysdot
5-Amino-2-bromo-4-nitrophenol 95+%
10g
$ 384.00

Chemenu
5-Amino-2-bromo-4-nitrophenol 95%
10g
$ 363.00

Chemenu
5-Amino-2-bromo-4-nitrophenol 95%
25g
$ 640.00

Alichem
5-Amino-2-bromo-4-nitrophenol
25g
$ 677.16

Alichem
5-Amino-2-bromo-4-nitrophenol
10g
$ 403.52

Total 7 raw suppliers

Chemical Property of 5-Amino-2-bromo-4-nitrophenol

Chemical Property:

PSA：92.07000
LogP:2.74950
Storage Temp.:Room temperature.
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:231.94835
Heavy Atom Count:12
Complexity:184

Purity/Quality:

97% ^*data from raw suppliers

5-Amino-2-bromo-4-nitrophenol 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C(=CC(=C1O)Br)[N+](=O)[O-])N

Technology Process of 5-Amino-2-bromo-4-nitrophenol

There total 2 articles about 5-Amino-2-bromo-4-nitrophenol 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:

: 860745-61-5
acetic acid-(4-bromo-5-hydroxy-2-nitro-anilide)

: 855836-08-7
5-amino-2-bromo-4-nitro-phenol

Guidance literature:: With potassium hydroxide;

Reference yield:

: 67915-26-8
N-(5-hydroxy-2-nitrophenyl)acetamide

: 855836-08-7
5-amino-2-bromo-4-nitro-phenol

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid; bromine

2: aq.-ethanolic KOH-solution

With potassium hydroxide; bromine; acetic acid;