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Encyclopedia

Artemotil

Base Information Edit
  • Chemical Name:Artemotil
  • CAS No.:75887-54-6
  • Molecular Formula:C17H28O5
  • Molecular Weight:312.406
  • Hs Code.:
  • UNII:XGL7GFB9YI
  • Nikkaji Number:J362.163D
  • Wikipedia:Artemotil
  • Wikidata:Q72443831
  • NCI Thesaurus Code:C73002
  • Metabolomics Workbench ID:154629
  • ChEMBL ID:CHEMBL301267
  • Mol file:75887-54-6.mol
Artemotil

Synonyms:arteether;arteether, (3R-(3alpha,5abeta,6beta,8abeta,9alpha,10alpha,12beta,12aR*))-isomer;arteether, (3R-(3alpha,5abeta,6beta,8abeta,9alpha,10beta,12beta,12aR*))-isomer;artemotil;artether;beta-artether;SM-227

Suppliers and Price of Artemotil
Supply Marketing:Edit
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
  • TRC
  • Arteether
  • 25mg
  • $ 285.00
  • TRC
  • Arteether
  • 100mg
  • $ 970.00
  • Medical Isotopes, Inc.
  • Arteether
  • 50 mg
  • $ 2000.00
  • Labseeker
  • Arteether 98
  • 1g
  • $ 308.00
  • CSNpharm
  • Arteether
  • 25mg
  • $ 125.00
  • CSNpharm
  • Arteether
  • 10mg
  • $ 68.00
  • CSNpharm
  • Arteether
  • 1mg
  • $ 35.00
  • CSNpharm
  • Arteether
  • 50mg
  • $ 238.00
  • Crysdot
  • Arteether 98+%
  • 100mg
  • $ 384.00
  • Crysdot
  • Arteether 98+%
  • 50mg
  • $ 224.00
Total 110 raw suppliers
Chemical Property of Artemotil Edit
Chemical Property:
  • Appearance/Colour:white crystalline solid 
  • Vapor Pressure:2.06E-05mmHg at 25°C 
  • Melting Point:80-820 °C 
  • Refractive Index:1.516 
  • Boiling Point:372.4 °C at 760 mmHg 
  • Flash Point:146 °C 
  • PSA:46.15000 
  • Density:1.16 g/cm3 
  • LogP:3.23090 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:312.19367399
  • Heavy Atom Count:22
  • Complexity:443
Purity/Quality:

99% *data from raw suppliers

Arteether *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC1C(C2CCC(C3C24C(O1)OC(CC3)(OO4)C)C)C
  • Isomeric SMILES:CCO[C@@H]1[C@@H]([C@@H]2CC[C@H]([C@H]3[C@]24[C@H](O1)O[C@@](CC3)(OO4)C)C)C
  • Description Arteether reached the market in the Netherlands as a solution in sesame oil, administered by i.m. injection, for the treatment of severe malaria infections in children and adolescents. Artheether, a sesquiterpene acetal with an endoperoxide bridge, is an ether derivative of the naturally occuring compound artemisinin, the active component of Chinese herbal remedies. As the other structural analogs of artemisinin, such as artesunate or artemether, it acts rapidly against Plasmodium, the parasite responsible for the disease, during the early blood stage of its development. It also exhibits a gametocytocidal activity against Plasmodium falciparum, reducing its potential for transmission. Because the only controlled clinical studies had been performed in children and adolescents, this new antimalarial drug was only approved for young patients. Further studies in adults treated with 150 mg i.m. artemotil, once daily for three consecutive days, indicated that the drug was efficient, rapidly acting (parasite clearance time meanly 38 h) and well tolerated. A new promising achievement in the regression of malaria is the combination of artemisinin derivatives with other long-lived antimalarials as mefloquine or pyrimethamine/sulfa.
  • Uses Derivative of Artemisinin. Antimalarial
Technology Process of Artemotil

There total 20 articles about Artemotil 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:
chloromethyldimethylsilane; In ethanol; at 20 - 23 ℃; for 0.666667 - 1.83333h; Acidic conditions;
Guidance literature:
With 2,2'-azobis(isobutyronitrile); n-Bu3SnH4; In toluene; for 20h; Heating;
DOI:10.1016/0223-5234(96)88287-0
Guidance literature:
With boron trifluoride diethyl etherate; In benzene; for 1h; Heating;
DOI:10.1021/jm00398a026
Refernces Edit
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