n-(4-Nitrophenyl)-1,3-benzothiazol-2-amine

Base Information

Chemical Name:n-(4-Nitrophenyl)-1,3-benzothiazol-2-amine
CAS No.:2501-06-6
Molecular Formula:C13H9N3O2S
Molecular Weight:271.299
Hs Code.:
NSC Number:34444
DSSTox Substance ID:DTXSID50283947
Nikkaji Number:J2.752.568G
Wikidata:Q82018708
ChEMBL ID:CHEMBL1448896
Mol file:2501-06-6.mol

Synonyms:NSC34444;NSC-34444;2501-06-6;n-(4-nitrophenyl)-1,3-benzothiazol-2-amine;NCIStruc1_000540;NCIStruc2_000526;SCHEMBL3490813;CHEMBL1448896;DTXSID50283947;NCI34444;CCG-37818;NCGC00013395;AKOS000125580;NCGC00013395-02;NCGC00096511-01;NCI60_003058;2-(4-(hydroxy(oxido)amino)anilino)-1,3-benzothiazole

Suppliers and Price of n-(4-Nitrophenyl)-1,3-benzothiazol-2-amine

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 6 raw suppliers

Chemical Property of n-(4-Nitrophenyl)-1,3-benzothiazol-2-amine

Chemical Property:

Vapor Pressure:1.48E-08mmHg at 25°C
Boiling Point:457.5°Cat760mmHg
Flash Point:230.5°C
PSA：98.98000
Density:1.473g/cm³
LogP:4.54430
XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:271.04154771
Heavy Atom Count:19
Complexity:328

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)N=C(S2)NC3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of n-(4-Nitrophenyl)-1,3-benzothiazol-2-amine

There total 10 articles about n-(4-Nitrophenyl)-1,3-benzothiazol-2-amine 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: 98.0%

: 615-43-0
2-iodophenylamine

: 2131-61-5
p-nitrophenyl isothiocyanate

: 2501-06-6
N-(4-nitrophenyl)benzo[d]thiazole-2-amine

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; iron(III) chloride; 1,10-Phenanthroline; trimethyloctadecylammonium chloride; In water; at 80 ℃;
DOI:10.1039/c0gc00123f

Reference yield: 98.0%

: 2131-61-5
p-nitrophenyl isothiocyanate

: 615-36-1
2-bromoaniline

: 2501-06-6
N-(4-nitrophenyl)benzo[d]thiazole-2-amine

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; In toluene; at 60 ℃; for 8h;
DOI:10.1016/j.tet.2011.05.121

Reference yield: 94.0%

: 137-07-5
2-amino-benzenethiol

: 2131-61-5
p-nitrophenyl isothiocyanate

: 2501-06-6
N-(4-nitrophenyl)benzo[d]thiazole-2-amine

Guidance literature:: With mutagenized vitreoscilla hemoglobin incorporating a cobalt porphyrin cofactor; air; In water; dimethyl sulfoxide; at 20 ℃; for 12h; Green chemistry;
DOI:10.1039/d1gc02533c