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Technology Process of Atovaquone-d5

Atovaquone-d5

Base Information
  • Chemical Name:Atovaquone-d5
  • CAS No.:1329792-63-3
  • Molecular Formula:C22H19ClO3
  • Molecular Weight:371.9
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10675642
  • Mol file:1329792-63-3.mol
Atovaquone-d5

Synonyms:Atovaquone-d5;1217612-80-0;1329792-63-3;cis-Atovaquone-d5 (contains 10% trans isomer);3-[4-(4-chlorophenyl)-1,2,2,6,6-pentadeuteriocyclohexyl]-4-hydroxynaphthalene-1,2-dione;cis-Atovaquone-d5 (contains 10per cent trans isomer);DTXSID10675642;cis-2-[4-(4-Chlorophenyl)cyclohexyl-d5-]-3-hydroxy-1,4-naphthalenedione-d5;HY-13832S2;CS-0202297;3-[4-(4-Chlorophenyl)(1,2,2,6,6-~2~H_5_)cyclohexyl]-4-hydroxynaphthalene-1,2-dione

Suppliers and Price of Atovaquone-d5
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
  • TRC
  • Atovaquone-d5
  • 5mg
  • $ 2080.00
  • Medical Isotopes, Inc.
  • Atovaquone-d5
  • 1 mg
  • $ 925.00
  • Medical Isotopes, Inc.
  • Atovaquone-d5
  • 5 mg
  • $ 2400.00
  • American Custom Chemicals Corporation
  • ATOVAQUONE-D5 95.00%
  • 5MG
  • $ 504.30
  • A2B
  • Atovaquone-d5
  • 5mg
  • $ 1851.00
  • A2B
  • Atovaquone-d5
  • 2.5mg
  • $ 1050.00
  • A2B
  • Atovaquone-d5
  • 1mg
  • $ 533.00
Total 4 raw suppliers
Chemical Property of Atovaquone-d5
Chemical Property:
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly) 
  • XLogP3:5.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:371.1336559
  • Heavy Atom Count:26
  • Complexity:595
Purity/Quality:

> 98% *data from raw suppliers

Atovaquone-d5 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CC(CCC1C2=CC=C(C=C2)Cl)C3=C(C4=CC=CC=C4C(=O)C3=O)O
  • Isomeric SMILES:[2H]C1(CC(CC(C1([2H])C2=C(C3=CC=CC=C3C(=O)C2=O)O)([2H])[2H])C4=CC=C(C=C4)Cl)[2H]
  • Uses Hydroxynaphthoquinone derivative that inhibits mitochondrial electron transport. Antipneumocystic
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Total 8 Pictures about this product