Oxireno(g)-1,2-benzisoxazole, 3a,4,5,5a,6a,6b-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-

Base Information

Chemical Name:Oxireno(g)-1,2-benzisoxazole, 3a,4,5,5a,6a,6b-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-
CAS No.:70483-68-0
Molecular Formula:C11H12N4O4
Molecular Weight:264.2374
Hs Code.:
DSSTox Substance ID:DTXSID60990690

Synonyms:Oxireno(g)-1,2-benzisoxazole, 3a,4,5,5a,6a,6b-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-;70483-68-0;NIOSH/DE4926500;DE49265000;Benzisoxazole, 3a,4,5,6,7,7a-hexahydro-6,7-epoxy-3-(1-methyl-5-nitroimidazol-2-yl)-;3a,4,5,6,7,7a-Hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-1,2-benzisoxazol-6,7-epoxide;SCHEMBL11274747;DTXSID60990690;3-(1-methyl-5-nitro-1H-imidazol-2-yl)-3a,4,5,5a,6a,6b-hexahydrooxireno[g][1,2]benzoxazole

Suppliers and Price of Oxireno(g)-1,2-benzisoxazole, 3a,4,5,5a,6a,6b-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-

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 1 raw suppliers

Chemical Property of Oxireno(g)-1,2-benzisoxazole, 3a,4,5,5a,6a,6b-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-

Chemical Property:

Vapor Pressure:2.11E-09mmHg at 25°C
Boiling Point:480.8°Cat760mmHg
Flash Point:244.6°C
Density:1.98g/cm³
XLogP3:0.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:264.08585488
Heavy Atom Count:19
Complexity:451

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C(=CN=C1C2=NOC3C2CCC4C3O4)[N+](=O)[O-]

Technology Process of Oxireno(g)-1,2-benzisoxazole, 3a,4,5,5a,6a,6b-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-

There total 4 articles about Oxireno(g)-1,2-benzisoxazole, 3a,4,5,5a,6a,6b-hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)- 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:

: 70483-67-9
3-(1-methyl-5-nitroimidazol-2-yl)-3a,4,5,7a-tetrahydro-1,2-benzisoxazole

: 70483-68-0
2-(3a,4,5,6,7,7a-hexahydro-6,7-oxido-1,2-benzisoxazol-3-yl)-1-methyl-5-nitroimidazole

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In HCCl₃;

Reference yield:

: 1-methyl-5-nitroimidazol-2-hydroxamic acid chloride

: 70483-68-0
2-(3a,4,5,6,7,7a-hexahydro-6,7-oxido-1,2-benzisoxazol-3-yl)-1-methyl-5-nitroimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran; HCCl₃

2: 3-chloro-benzenecarboperoxoic acid / HCCl₃

With triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; HCCl₃;

Reference yield:

: 1165952-91-9
cyclohexa-1,3-diene

: 70483-68-0
2-(3a,4,5,6,7,7a-hexahydro-6,7-oxido-1,2-benzisoxazol-3-yl)-1-methyl-5-nitroimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran; HCCl₃

2: 3-chloro-benzenecarboperoxoic acid / HCCl₃

With triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; HCCl₃;