Phenazine, 1,2,3,4-tetrahydro-, 5,10-dioxide

Base Information

Chemical Name:Phenazine, 1,2,3,4-tetrahydro-, 5,10-dioxide
CAS No.:4121-35-1
Molecular Formula:C12H12 N2 O2
Molecular Weight:216.239
Hs Code.:2933990090
NSC Number:39304
DSSTox Substance ID:DTXSID40194134
Nikkaji Number:J3.006.529H
Wikidata:Q83066889
ChEMBL ID:CHEMBL1370774
Mol file:4121-35-1.mol

Synonyms:1,2,3,4-tetrahydrophenazine 5,10-dioxide;4121-35-1;Phenazine, 1,2,3,4-tetrahydro-, 5,10-dioxide;1,2,3,4-Tetrahydrophenazine-di-N-oxide;HMS2450M04;NSC39304;MLS000532025;CHEMBL1370774;SCHEMBL10902440;DTXSID40194134;NSC-39304;STK763246;AKOS005614515;SDCCGMLS-0064713.P001;NCGC00245741-01;SMR000136967;LS-103023;1,2,3,4-tetrahydro-phenazine 5,10-dioxide;SR-01000204202;SR-01000204202-1;5,10-dioxido-1,2,3,4-tetrahydro-phenazine-5,10-diium

Suppliers and Price of Phenazine, 1,2,3,4-tetrahydro-, 5,10-dioxide

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

American Custom Chemicals Corporation
1,2,3,4-TETRAHYDROPHENAZINE-DI-N-OXIDE 95.00%
5MG
$ 501.42

Total 5 raw suppliers

Chemical Property of Phenazine, 1,2,3,4-tetrahydro-, 5,10-dioxide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：50.92000
Density:g/cm³
LogP:2.57560
XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:216.089877630
Heavy Atom Count:16
Complexity:319

Purity/Quality:: 1,2,3,4-TETRAHYDROPHENAZINE-DI-N-OXIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC2=C(C1)N(C3=CC=CC=C3[N+]2=O)[O-]

Technology Process of Phenazine, 1,2,3,4-tetrahydro-, 5,10-dioxide

There total 5 articles about Phenazine, 1,2,3,4-tetrahydro-, 5,10-dioxide 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: 91.0%

: 4829-73-6
1,2,3,4-tetrahydrophenazine

: 4121-35-1
1,2,3,4-tetrahydro-5,10-phenazine N,N'-dioxide

: 19366-60-0
mono-N-oxide of 1,2,3,4-tetrahydrophenazine

Guidance literature:: With Perbenzoic acid; In chloroform; at 0 ℃; for 72h;

Reference yield: 71.0%

: 480-96-6,68100-26-5
benzofurazan oxide

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 4121-35-1
1,2,3,4-tetrahydro-5,10-phenazine N,N'-dioxide

Guidance literature:: benzofurazan oxide; With β‐cyclodextrin; In methanol; water; for 0.5h;

cyclohexanone; In methanol; water; at 20 ℃; for 0.75h;
DOI:10.1080/00397911.2010.517371