Bufalitoxin

Base Information

Chemical Name:Bufalitoxin
CAS No.:35455-33-5
Molecular Formula:C38H58N4O8
Molecular Weight:698.901
Hs Code.:
Nikkaji Number:J82.333C
Wikidata:Q104981730
Mol file:35455-33-5.mol

Synonyms:NSC 248524;Bufa-20,22-dienolide, 3-((8-((4-((aminoiminomethyl)amino)-1-carboxybutyl)amino)-1,8-dioxooctyl)oxy)-14-hydroxy-, (3beta(S),5beta)-

Suppliers and Price of Bufalitoxin

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

Total 2 raw suppliers

Chemical Property of Bufalitoxin

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：205.04000
Density:1.35g/cm³
LogP:6.54790
XLogP3:4.1
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:16
Exact Mass:698.42546482
Heavy Atom Count:50
Complexity:1380

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=COC(=O)C=C5)O)C)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O
Isomeric SMILES:C[C@]12CC[C@@H](C[C@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@@]3(CC[C@@H]4C5=COC(=O)C=C5)O)C)OC(=O)CCCCCCC(=O)N[C@@H](CCCN=C(N)N)C(=O)O

Technology Process of Bufalitoxin

There total 1 articles about Bufalitoxin 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:

: 465-21-4
5-((3S,5R,8R,9S,10S,13R,14S)-3,14-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2H-pyran-2-one

: 35455-33-5
bufalitoxin

Guidance literature:: Multi-step reaction with 2 steps

1: 0.125 g / pyridine / 6 h / Heating

2: 1.) triethylamine, 2.) isobutyl chloroformate

With pyridine; triethylamine; isobutyl chloroformate;
DOI:10.1021/jo00392a014