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Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, L-

Base Information
  • Chemical Name:Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, L-
  • CAS No.:81176-34-3
  • Molecular Formula:C32H49NO9
  • Molecular Weight:591.742
  • Hs Code.:
  • Mol file:81176-34-3.mol
Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, L-

Synonyms:81072-30-2;Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, L-;Digitoxigenin-3-beta-N-D-(6-deoxy-L-mannosyl)alanyl ester;Digitoxigenin-3-beta-N-L-(6-deoxy-L-mannosyl)alanyl ester;Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, D-;Digitoxigenin 3beta-N-D-(6-deoxy-L-mannosyl)alanyl ester;81176-34-3;LS-15995;LS-15996;[14-Hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]2-(2,3,4,5-tetrahydroxyhexylideneamino)propanoate

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Chemical Property of Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, L-
Chemical Property:
  • Vapor Pressure:8.78E-30mmHg at 25°C 
  • Boiling Point:802.4°Cat760mmHg 
  • Flash Point:439.1°C 
  • PSA:0.00000 
  • Density:1.42g/cm3 
  • LogP:0.00000 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:9
  • Exact Mass:591.34073214
  • Heavy Atom Count:42
  • Complexity:1110
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C(C(C(C=NC(C)C(=O)OC1CCC2(C(C1)CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)C)O)O)O)O
Technology Process of Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, L-

There total 4 articles about Alanine, N-(6-deoxy-L-mannosyl)-, 3-ester with 3-beta,14-dihydroxy-5-beta-card-20(22)-enolide, L- 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:
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