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Anthrylmethyl okadaate

Base Information
  • Chemical Name:Anthrylmethyl okadaate
  • CAS No.:157606-35-4
  • Molecular Formula:C59H78O13
  • Molecular Weight:995.261
  • Hs Code.:
  • European Community (EC) Number:633-891-5
  • Mol file:157606-35-4.mol
Anthrylmethyl okadaate

Synonyms:ANTHRYLMETHYL OKADAATE;157606-35-4;Anthracen-9-ylmethyl 2-hydroxy-3-[11-hydroxy-2-[(E)-4-[4-hydroxy-2-[1-hydroxy-3-(3-methyl-1,7-dioxaspiro[5.5]undecan-2-yl)butyl]-3-methylidenespiro[4a,7,8,8a-tetrahydro-4H-pyrano[3,2-b]pyran-6,5'-oxolane]-2'-yl]but-3-en-2-yl]-4-methyl-1,7-dioxaspiro[5.5]undec-4-en-8-yl]-2-methylpropanoate

Suppliers and Price of Anthrylmethyl okadaate
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
  • AnthrylmethylOkadaate
  • 25μg
  • $ 285.00
  • TRC
  • AnthrylmethylOkadaate
  • 10μg
  • $ 145.00
Total 2 raw suppliers
Chemical Property of Anthrylmethyl okadaate
Chemical Property:
  • PSA:171.83000 
  • LogP:9.17880 
  • Storage Temp.:?20°C 
  • XLogP3:7.7
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:13
  • Rotatable Bond Count:13
  • Exact Mass:994.54424254
  • Heavy Atom Count:72
  • Complexity:1940
Purity/Quality:

99% *data from raw suppliers

AnthrylmethylOkadaate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 20/21/22-38 
  • Safety Statements: 22-26-36/37/39-45 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1CCC2(CCCCO2)OC1C(C)CC(C3C(=C)C(C4C(O3)CCC5(O4)CCC(O5)C=CC(C)C6CC(=CC7(O6)C(CCC(O7)CC(C)(C(=O)OCC8=C9C=CC=CC9=CC1=CC=CC=C18)O)O)C)O)O
  • Isomeric SMILES:CC1CCC2(CCCCO2)OC1C(C)CC(C3C(=C)C(C4C(O3)CCC5(O4)CCC(O5)/C=C/C(C)C6CC(=CC7(O6)C(CCC(O7)CC(C)(C(=O)OCC8=C9C=CC=CC9=CC1=CC=CC=C18)O)O)C)O)O
  • Uses Okadaic Acid 9-Anthrylmethyl Ester is a standard useful in the analysis of okadaic acid (CAT# O515500), which is a widely distributed marine toxin produced by several phytoplanktonic species and a potent and specific inhibitor of various types of serine/threonine protein phosphatases.
Technology Process of Anthrylmethyl okadaate

There total 1 articles about Anthrylmethyl okadaate 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:
In methanol; for 2h; Ambient temperature;
upstream raw materials:

9-anthryldiazomethane

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