N-tert-Butyl-2-nitroaniline

Base Information

Chemical Name:N-tert-Butyl-2-nitroaniline
CAS No.:28458-45-9
Molecular Formula:C10H14N2O2
Molecular Weight:194.233
Hs Code.:2921420090
DSSTox Substance ID:DTXSID50445003
Nikkaji Number:J650.854E
Mol file:28458-45-9.mol

Synonyms:N-tert-Butyl-2-nitroaniline;28458-45-9;N-(tert-Butyl)-2-nitroaniline;N-t-butyl-2-nitroaniline;2-nitro-N-tert-butylaniline;SCHEMBL677655;DTXSID50445003;HIGVOOQGROZGET-UHFFFAOYSA-N;tert-butyl-(2-nitrophenyl)-amine;tert-Butyl-(2-nitro-phenyl)-amine;AC5803;MFCD16170799;AKOS005209172;BS-22200;SY039309;CS-0208144;Z31213820;F1911-3562

Suppliers and Price of N-tert-Butyl-2-nitroaniline

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
N-(tert-Butyl)-2-nitroaniline 95+%
25g
$ 301.00

Crysdot
N-(tert-Butyl)-2-nitroaniline 95+%
100g
$ 790.00

Apolloscientific
N-tert-Butyl-2-nitroaniline 98%
25g
$ 573.00

Apolloscientific
N-tert-Butyl-2-nitroaniline 98%
5g
$ 269.00

Apolloscientific
N-tert-Butyl-2-nitroaniline 98%
1g
$ 145.00

Total 5 raw suppliers

Chemical Property of N-tert-Butyl-2-nitroaniline

Chemical Property:

PSA：57.85000
LogP:3.40140
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:194.105527694
Heavy Atom Count:14
Complexity:205

Purity/Quality:

97% ^*data from raw suppliers

N-(tert-Butyl)-2-nitroaniline 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)NC1=CC=CC=C1[N+](=O)[O-]
Uses N-Tert-butyl-2-nitroaniline is used as a reactant in the preparation of benzimidazol-2-ones as potent, selective, and orally efficacious norepinephrine reuptake inhibitors.

Technology Process of N-tert-Butyl-2-nitroaniline

There total 5 articles about N-tert-Butyl-2-nitroaniline 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: 99.0%