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TR-2 Mycotoxin

Base Information
  • Chemical Name:TR-2 Mycotoxin
  • CAS No.:51177-07-2
  • Molecular Formula:C22H27N3O6
  • Molecular Weight:429.4663
  • Hs Code.:
  • NSC Number:353637
  • UNII:RTC582PPE3
  • DSSTox Substance ID:DTXSID901017899
  • Wikidata:Q105209759
  • Metabolomics Workbench ID:107200
  • Mol file:51177-07-2.mol
TR-2 Mycotoxin

Synonyms:TR 2;TR-2 mycotoxin

Suppliers and Price of TR-2 Mycotoxin
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 3 raw suppliers
Chemical Property of TR-2 Mycotoxin
Chemical Property:
  • Boiling Point:756.1°Cat760mmHg 
  • Flash Point:411.1°C 
  • PSA:126.33000 
  • Density:1.52g/cm3 
  • LogP:0.82320 
  • XLogP3:-0.3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:429.18998559
  • Heavy Atom Count:31
  • Complexity:776
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(CC1C2=C(C(C3(N1C(=O)C4CCCN4C3=O)O)O)C5=C(N2)C=C(C=C5)OC)O
  • Isomeric SMILES:CC(C)(C[C@H]1C2=C([C@@H]([C@@]3(N1C(=O)[C@@H]4CCCN4C3=O)O)O)C5=C(N2)C=C(C=C5)OC)O
Technology Process of TR-2 Mycotoxin

There total 3 articles about TR-2 Mycotoxin 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 osmium(VIII) oxide; In pyridine;
DOI:10.1016/S0040-4039(00)80288-9
Guidance literature:
Multi-step reaction with 3 steps
1: 73 percent / 2,3,4,5,6,6-hexachloro-2,4-cyclohexadien-1-one / CH2Cl2 / 0.5 h
2: 46 percent / trifluoroacetic acid / CH2Cl2 / 1 h / Ambient temperature
3: 1) osmium tetroxide, 2) aq. NaHSO3 / 1) pyridine, 0 deg C, 2 h, 2) room temperature, 30 min
With osmium(VIII) oxide; 2,2,3,4,5,6-hexachloro-cyclohexa-2,4-dien-1-one; sodium hydrogensulfite; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/jo00040a030
Guidance literature:
Multi-step reaction with 2 steps
1: 46 percent / trifluoroacetic acid / CH2Cl2 / 1 h / Ambient temperature
2: 1) osmium tetroxide, 2) aq. NaHSO3 / 1) pyridine, 0 deg C, 2 h, 2) room temperature, 30 min
With osmium(VIII) oxide; sodium hydrogensulfite; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/jo00040a030
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