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Trioxidane

Base Information
  • Chemical Name:Trioxidane
  • CAS No.:14699-99-1
  • Molecular Formula:H2O3
  • Molecular Weight:50.0141
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60932994
  • Nikkaji Number:J1.680.850D
  • Wikipedia:Trioxidane
  • Wikidata:Q417642,Q27110056
  • RXCUI:1310514
  • Mol file:14699-99-1.mol
Trioxidane

Synonyms:trioxidane;epoxy alcohol;ketoalcohol;oxoalcohol;Lactoperoxidase;Dihydroxy ether;HOOOH;Horseradish peroxidase;Horse radish peroxidase;Myeloperoxidase, human pmn;UNII-JQZ6YM58U5;UNII-2TQ44G23HV;CHEBI:46736;DTXSID60932994;EINECS 232-668-6;14699-99-1;EC 1.11.1.7;E.C. 1.11.1.7;Q417642;Q27110056

Suppliers and Price of Trioxidane
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 7 raw suppliers
Chemical Property of Trioxidane
Chemical Property:
  • PSA:49.69000 
  • LogP:-0.05100 
  • XLogP3:-0.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:50.000393922
  • Heavy Atom Count:3
  • Complexity:0
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:OOO
Technology Process of Trioxidane

There total 16 articles about Trioxidane 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 methytrioxorhenium(VII); at -30 ℃; for 3h; polystyrene bead
DOI:10.1002/anie.201504084
Guidance literature:
In acetic acid methyl ester; ozonation od 1,2-diphenylhydrazine with ozone-nitrogen or ozone-oxygen mixt. in methyl acetate at -78°C;
DOI:10.1021/ja036801u
Guidance literature:
In [(2)H6]acetone; byproducts: PhN(O)NPh; ozonation od 1,2-diphenylhydrazine with ozone-nitrogen or ozone-oxygen mixt. in acetone-d6 at -60°C; monitoring by NMR;
DOI:10.1021/ja036801u
Refernces

Total Synthesis of Prostaglandin F via Nickel-Promoted Stereoselective Cyclization of 1,3-Diene and Aldehyde

10.1055/s-1997-3268

The research aims to achieve the total synthesis of prostaglandin F2a (PGF2a) using a nickel-promoted cyclization method. The study employs key chemicals such as 1,3-cyclohexadiene (1,3-CHD), hydride nickel complex generated from Ni(acac)2 and PPh3, and various reagents like DIBAL-H, PCC, and Wittig reagents. The researchers successfully synthesized PGF2a by first preparing an optically active substrate (16) from chiral epoxy alcohol (10). This substrate underwent nickel-promoted cyclization in the presence of 1,3-CHD to stereoselectively form the key intermediate (18), which contains the a-chain and four contiguous chiral carbon centers of PGF2a. The intermediate was then transformed into PGF2a through a series of reactions. The study concludes that nickel-promoted cyclization is a promising method for constructing cyclopentanoids and provides a new approach for the synthesis of PGF2a, with further studies ongoing to explore its potential.

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