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Anaxirone

Base Information
  • Chemical Name:Anaxirone
  • CAS No.:77658-97-0
  • Molecular Formula:C11H15N3O5
  • Molecular Weight:269.257
  • Hs Code.:
  • European Community (EC) Number:278-745-8
  • NSC Number:332488
  • UNII:36R61Y789T
  • DSSTox Substance ID:DTXSID10868451
  • Nikkaji Number:J22.779J
  • Wikidata:Q27256591
  • NCI Thesaurus Code:C950
  • Metabolomics Workbench ID:155801
  • ChEMBL ID:CHEMBL2105991
  • Mol file:77658-97-0.mol
Anaxirone

Synonyms:1,2,4-TGU;1,2,4-triglycidyl urazol;anaxirone;NSC 332488

Suppliers and Price of Anaxirone
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
  • ANAXIRONE 95.00%
  • 5MG
  • $ 504.54
Total 9 raw suppliers
Chemical Property of Anaxirone
Chemical Property:
  • Vapor Pressure:8.51E-07mmHg at 25°C 
  • Melting Point:91°C 
  • Refractive Index:1.4930 (estimate) 
  • Boiling Point:405.8°C at 760 mmHg 
  • Flash Point:199.2°C 
  • PSA:86.52000 
  • Density:1.596g/cm3 
  • LogP:-1.99210 
  • Water Solubility.:0.2g/L(temperature not stated) 
  • XLogP3:-1.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:269.10117059
  • Heavy Atom Count:19
  • Complexity:399
Purity/Quality:

99% *data from raw suppliers

ANAXIRONE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(O1)CN2C(=O)N(N(C2=O)CC3CO3)CC4CO4
  • Uses Triglycidylurazole is a drug shown to reduce tumor-induced bone destruction in the rat.
  • Therapeutic Function Antineoplastic
Technology Process of Anaxirone

There total 2 articles about Anaxirone 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 hydroxide; quaternary ammonium salt; Yield given. Multistep reaction; 1.) 60 - 116 deg C;
Guidance literature:
With tetraethylammonium chloride; at 100 ℃; for 1h;
DOI:10.1007/BF00772856
upstream raw materials:

urazole

epichlorohydrin

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