Digitoxigenin digitoxoside

Base Information

Chemical Name:Digitoxigenin digitoxoside
CAS No.:18404-43-8
Molecular Formula:C29H44 O7
Molecular Weight:504.664
Hs Code.:
European Community (EC) Number:242-284-0
DSSTox Substance ID:DTXSID50939790
Mol file:18404-43-8.mol

Synonyms:digitoxigenin monodigitoxoside;digitoxigenin monodigitoxoside, (arabino-3beta,5alpha)-isomer;digitoxigenin monodigitoxoside, (ribo-3beta,5alpha)-isomer

Suppliers and Price of Digitoxigenin digitoxoside

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
DigitoxigeninMono-β-D-digitoxoside
0.5mg
$ 120.00

Total 5 raw suppliers

Chemical Property of Digitoxigenin digitoxoside

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:673.3°Cat760mmHg
Flash Point:218.5°C
PSA：105.45000
Density:1.27g/cm³
LogP:3.48530
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
XLogP3:2.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:3
Exact Mass:504.30870374
Heavy Atom Count:36
Complexity:919

Purity/Quality:

99% ^*data from raw suppliers

DigitoxigeninMono-β-D-digitoxoside ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)O
Isomeric SMILES:CC1[C@H](C(C[C@@H](O1)O[C@H]2CC[C@]3([C@@H](C2)CCC4C3CC[C@]5([C@@]4(CC[C@@H]5C6=CC(=O)OC6)O)C)C)O)O
Uses Digitoxigenin Mono-β-D-digitoxoside is a cardenolides which possesses cytotoxic, anti-migratory, anti-invasive and anti-proliferative effects in all tumor cells.

Technology Process of Digitoxigenin digitoxoside

There total 20 articles about Digitoxigenin digitoxoside 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:

Reference yield: 93.0%

: 912454-91-2
(2R,6R)-2-(digitoxigenoxy)-3,6-dihydro-6-methyl-2H-pyran

: 18404-43-8
evatromonoside

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; tert-butyl alcohol; at 0 ℃; for 4h;
DOI:10.1021/ol061683b

Reference yield: 86.0%

: C₆₁H₈₀O₇Si₂

: 67375-01-3
(Digitoxigenin-3-yl)-2,6-didesoxy-α-D-ribo-hexopyranosid

: 18404-43-8
evatromonoside

Guidance literature:: With ammonium fluoride-hydrogen fluoride; In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide; at 70 ℃; for 120h; Inert atmosphere;
DOI:10.1021/jo201850z

Reference yield: 84.0%

: 16479-50-8
digitoxigen O-[2',6'-dideoxy-β-D-ribo-hexopyranosyl]-(1->4)-(2,6-dideoxy-β-D-ribo-hexopyranoside)

: 18404-43-8
evatromonoside

Guidance literature:: digitoxigen O-[2',6'-dideoxy-β-D-ribo-hexopyranosyl]-(1->4)-(2,6-dideoxy-β-D-ribo-hexopyranoside); With sodium periodate; In ethanol; water;

With methanol; sodium tetrahydroborate; for 4h;

With hydrogenchloride; In methanol; water;
DOI:10.1055/s-0043-109557