Chlorsulfaquinoxaline

Base Information

Chemical Name:Chlorsulfaquinoxaline
CAS No.:97919-22-7
Molecular Formula:C14H11 Cl N4 O2 S
Molecular Weight:334.786
Hs Code.:2935009090
NSC Number:339004
UNII:O0408QB48D
DSSTox Substance ID:DTXSID10243340
Nikkaji Number:J518.582C
Wikidata:Q27285146
NCI Thesaurus Code:C982
Metabolomics Workbench ID:153810
ChEMBL ID:CHEMBL1905073
Mol file:97919-22-7.mol

Synonyms:5-chloroquinoxaline-2-sulfanilamide;chloroquinoxaline sulfonamide;chlorsulfaquinoxaline;NSC-339004

Suppliers and Price of Chlorsulfaquinoxaline

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

TRC
Chlorsulfaquinoxaline
5mg
$ 150.00

ChemScene
Chloroquinoxalinesulfonamide 99.47%
50mg
$ 1050.00

ChemScene
Chloroquinoxalinesulfonamide 99.47%
25mg
$ 600.00

ChemScene
Chloroquinoxalinesulfonamide 99.47%
10mg
$ 300.00

ChemScene
Chloroquinoxalinesulfonamide 99.47%
5mg
$ 165.00

Total 8 raw suppliers

Chemical Property of Chlorsulfaquinoxaline

Chemical Property:

Vapor Pressure:2.79E-13mmHg at 25°C
Refractive Index:1.5630 (estimate)
Boiling Point:576.3°Cat760mmHg
Flash Point:302.3°C
PSA：106.35000
Density:1.569g/cm³
LogP:4.40120
Storage Temp.:Refrigerator
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:334.0291245
Heavy Atom Count:22
Complexity:476

Purity/Quality:

97% ^*data from raw suppliers

Chlorsulfaquinoxaline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=NC(=CN=C2C(=C1)Cl)NS(=O)(=O)C3=CC=C(C=C3)N
Recent ClinicalTrials:Chloroquinoxaline Sulfonamide in Treating Patients With Stage IV Colorectal Cancer
Uses Chlorsulfaquinoxaline is used to prepare carbonic anhydrase inhibitors 1,3,4-thiadiazole-2-sulfonamide derivatives as antitumor agents.

Technology Process of Chlorsulfaquinoxaline

There total 6 articles about Chlorsulfaquinoxaline 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:

: N-acetyl-sulfanilic acid-(5-chloro-quinoxalin-2-ylamide)

: 97919-22-7
4-amino-N-(5-chloro-2-quinoxalinyl)benzenesulfonamide

Guidance literature:: With sodium hydroxide; water;
DOI:10.1021/ja01169a001

Reference yield:

: 5-chloro-quinoxalin-2-ylamine

: 97919-22-7
4-amino-N-(5-chloro-2-quinoxalinyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine

2: water; NaOH

With pyridine; sodium hydroxide; water;
DOI:10.1021/ja01169a001

Reference yield:

: 55687-05-3
2,5-dichloroquinoxaline

: 97919-22-7
4-amino-N-(5-chloro-2-quinoxalinyl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol; NH₃

2: pyridine

3: water; NaOH

With pyridine; sodium hydroxide; ethanol; ammonia; water;
DOI:10.1021/ja01169a001