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Oxisuran

Base Information
  • Chemical Name:Oxisuran
  • CAS No.:27302-90-5
  • Molecular Formula:C8H9 N O2 S
  • Molecular Weight:183.24
  • Hs Code.:
  • NSC Number:356716
  • UNII:NJM3553DH2
  • DSSTox Substance ID:DTXSID60865359
  • Nikkaji Number:J10.722K
  • Wikidata:Q27284895
  • NCI Thesaurus Code:C90874
  • ChEMBL ID:CHEMBL2106596
  • Mol file:27302-90-5.mol
Oxisuran

Synonyms:(methylsulfinyl)methyl 2-pyridyl ketone;oxisuran

Suppliers and Price of Oxisuran
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
  • OXISURAN 95.00%
  • 5MG
  • $ 496.16
Total 8 raw suppliers
Chemical Property of Oxisuran
Chemical Property:
  • Vapor Pressure:7.08E-07mmHg at 25°C 
  • Melting Point:78-79 °C(Solv: ethyl acetate (141-78-6)) 
  • Refractive Index:1.5650 (estimate) 
  • Boiling Point:408.3°Cat760mmHg 
  • PKA:2.03±0.10(Predicted) 
  • Flash Point:200.7°C 
  • PSA:66.24000 
  • Density:1.306g/cm3 
  • LogP:1.50850 
  • XLogP3:0.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:183.03539970
  • Heavy Atom Count:12
  • Complexity:194
Purity/Quality:

99% *data from raw suppliers

OXISURAN 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CS(=O)CC(=O)C1=CC=CC=N1
  • Uses Antineoplastic.
Technology Process of Oxisuran

There total 4 articles about Oxisuran 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:
Guidance literature:
With sodium periodate; further reagent;
DOI:10.1016/S0040-4020(01)90316-3
Guidance literature:
Multi-step reaction with 2 steps
1: 97.5 percent / methanol / Ambient temperature
2: 93 percent / sodium metaperiodate / further reagent
With sodium periodate; In methanol;
DOI:10.1016/S0040-4020(01)90316-3
Guidance literature:
Multi-step reaction with 3 steps
1: 18.9 percent / bromine / benzene; acetic acid / 60 °C
2: 97.5 percent / methanol / Ambient temperature
3: 93 percent / sodium metaperiodate / further reagent
With sodium periodate; bromine; In methanol; acetic acid; benzene;
DOI:10.1016/S0040-4020(01)90316-3
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