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Tylvalosin

Base Information
  • Chemical Name:Tylvalosin
  • CAS No.:63409-12-1
  • Molecular Formula:C53H87NO19
  • Molecular Weight:1042.27
  • Hs Code.:
  • European Community (EC) Number:264-132-2
  • UNII:9T02S42WQO
  • DSSTox Substance ID:DTXSID901016510
  • Wikidata:Q27273124
  • NCI Thesaurus Code:C152787
  • Metabolomics Workbench ID:152712
  • ChEMBL ID:CHEMBL2103834
  • Mol file:63409-12-1.mol
Tylvalosin

Synonyms:tylvalosin

Suppliers and Price of Tylvalosin
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
  • Medical Isotopes, Inc.
  • Tylvalosin
  • 1 mg
  • $ 675.00
  • Medical Isotopes, Inc.
  • Tylvalosin
  • 10 mg
  • $ 2400.00
  • Biorbyt Ltd
  • Tylvalosin
  • 500 μg
  • $ 957.10
  • Biorbyt Ltd
  • Tylvalosin
  • 100 μg
  • $ 635.80
  • Biorbyt Ltd
  • Tylvalosin
  • 50 μg
  • $ 425.00
  • American Custom Chemicals Corporation
  • TYLVALOSIN 95.00%
  • 25MG
  • $ 5500.00
  • American Custom Chemicals Corporation
  • TYLVALOSIN 95.00%
  • 5MG
  • $ 2497.39
Total 19 raw suppliers
Chemical Property of Tylvalosin
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:>105°C (dec.) 
  • Boiling Point:1005.4°Cat760mmHg 
  • PKA:13.06±0.70(Predicted) 
  • Flash Point:561.8°C 
  • PSA:250.81000 
  • Density:1.21g/cm3 
  • LogP:4.00130 
  • Storage Temp.:-20°C Freezer, Under Inert Atmosphere 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:20
  • Rotatable Bond Count:19
  • Exact Mass:1041.58722955
  • Heavy Atom Count:73
  • Complexity:1860
Purity/Quality:

99%, *data from raw suppliers

Tylvalosin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC1C(C=C(C=CC(=O)C(CC(C(C(C(CC(=O)O1)OC(=O)C)C)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)OC(=O)CC(C)C)(C)O)N(C)C)O)CC=O)C)C)COC4C(C(C(C(O4)C)O)OC)OC
  • Isomeric SMILES:CC[C@@H]1[C@H](/C=C(/C=C/C(=O)[C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)OC(=O)C)C)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)OC(=O)CC(C)C)(C)O)N(C)C)O)CC=O)C)\C)CO[C@H]4[C@@H]([C@@H]([C@@H]([C@H](O4)C)O)OC)OC
  • Uses Tylvalosin is an anti-bacterial agent that is shown through study as a good inhibitor of gram-positive bacteria.
Technology Process of Tylvalosin

There total 6 articles about Tylvalosin 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 triethylamine; In methanol; at 25 ℃; for 67h;
DOI:10.1039/P19890000787
Guidance literature:
Multi-step reaction with 3 steps
1: 49 percent / 4-dimethylaminopyridine, triethylamine / CH2Cl2 / 18 h / 25 °C
2: 82 percent / 4-dimethylaminopyridine, triethylamine / CH2Cl2 / 21 h / 25 °C
3: 45 percent / triethylamine (33percent) / methanol / 66 h / 25 °C
With dmap; triethylamine; In methanol; dichloromethane;
DOI:10.1039/P19890000787
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