2-Bromo-5-nitro-1H-indole

Base Information

Chemical Name:2-Bromo-5-nitro-1H-indole
CAS No.:1246471-11-3
Molecular Formula:C8H5BrN2O2
Molecular Weight:241.044
Hs Code.:2933990090
DSSTox Substance ID:DTXSID20700075
Wikidata:Q82631255
Mol file:1246471-11-3.mol

Synonyms:2-BROMO-5-NITRO-1H-INDOLE;1246471-11-3;1H-Indole, 2-bromo-5-nitro-;SCHEMBL10172985;DTXSID20700075;WZB47111;MFCD22570488;AS-59007;CS-0375908;FT-0722712;C71973;EN300-4377738

Suppliers and Price of 2-Bromo-5-nitro-1H-indole

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

Matrix Scientific
2-Bromo-5-nitro-1H-indole 97%
10g
$ 2250.00

Matrix Scientific
2-Bromo-5-nitro-1H-indole 97%
5g
$ 1239.00

Crysdot
2-Bromo-5-nitro-1H-indole 95+%
5g
$ 749.00

Chemenu
2-Bromo-5-nitro-1H-indole 95%
5g
$ 707.00

American Custom Chemicals Corporation
2-BROMO-5-NITRO-1H-INDOLE 95.00%
1G
$ 599.55

Alichem
2-Bromo-5-nitro-1H-indole
1g
$ 400.00

AK Scientific
2-Bromo-5-nitro-1H-indole
1g
$ 323.00

Total 10 raw suppliers

Chemical Property of 2-Bromo-5-nitro-1H-indole

Chemical Property:

PSA：61.61000
LogP:3.36180
Storage Temp.:Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:239.95344
Heavy Atom Count:13
Complexity:219

Purity/Quality:

99%, ^*data from raw suppliers

2-Bromo-5-nitro-1H-indole 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C1[N+](=O)[O-])C=C(N2)Br

Technology Process of 2-Bromo-5-nitro-1H-indole

There total 1 articles about 2-Bromo-5-nitro-1H-indole 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: 54.0%

: 20870-79-5
5-nitrooxindole

: 1246471-11-3
2-bromo-5-nitro-1H-indole

Guidance literature:: 5-nitrooxindole; With phosphorus(V) oxybromide; In 1,2-dichloro-ethane; at 90 ℃; for 0.5h;

With 1H-imidazole; In 1,2-dichloro-ethane; at 90 ℃; for 2h;

Reference yield: 85.0%

: 1246471-11-3
2-bromo-5-nitro-1H-indole

: 74-88-4
methyl iodide

: 31521-56-9
1-methyl-5-nitro-2-phenyl-1H-indole

Guidance literature:: 2-bromo-5-nitro-1H-indole; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h;

methyl iodide; In N,N-dimethyl-formamide; at 20 ℃; for 1.5h;

Reference yield: 56.0%

: 1246471-11-3
2-bromo-5-nitro-1H-indole

: 98-80-6
phenylboronic acid

: 4993-87-7
5-nitro-2-phenyl-1H-indole

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; In 1,4-dioxane; at 100 ℃; for 12h;