Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Astragenol

Base Information Edit
  • Chemical Name:Astragenol
  • CAS No.:86541-79-9
  • Molecular Formula:C30H50O5
  • Molecular Weight:490.724
  • Hs Code.:
  • DSSTox Substance ID:DTXSID401170200
  • Nikkaji Number:J3.122.500K
  • Wikidata:Q104246816
  • Mol file:86541-79-9.mol
Astragenol

Synonyms:Astragenol;86541-79-9;DTXSID401170200;HY-N7924;MS-29123;CS-0138811;(3beta,6alpha,16beta,20R,24S)-20,24-Epoxylanost-9(11)-ene-3,6,16,25-tetrol;(3S,5R,6S,8S,10S,13R,14S,16S,17R)-17-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol

Suppliers and Price of Astragenol
Supply Marketing:Edit
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 18 raw suppliers
Chemical Property of Astragenol Edit
Chemical Property:
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:490.36582469
  • Heavy Atom Count:35
  • Complexity:910
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1(C(CCC2(C1C(CC3C2=CCC4(C3(CC(C4C5(CCC(O5)C(C)(C)O)C)O)C)C)O)C)O)C
  • Isomeric SMILES:C[C@@]1(CC[C@H](O1)C(C)(C)O)[C@H]2[C@H](C[C@@]3([C@@]2(CC=C4[C@H]3C[C@@H]([C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)O)C)C)O
Technology Process of Astragenol

There total 8 articles about Astragenol 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:
With sulfuric acid; In methanol; for 6h; Reflux;
DOI:10.1016/j.tetlet.2012.08.068
Guidance literature:
With sulfuric acid; In methanol; for 10h; Heating;
DOI:10.1248/cpb.31.698
Guidance literature:
Multi-step reaction with 2 steps
1: 45 mg / 1.) 10 percent sodium methoxide; 2.) Dowex 50w*8(H+) / methanol / 0.25 h / Heating
2: 34 mg / aq. 20 percent sulfuric acid / methanol / 10 h / Heating
With Dowex 50w*8(H+); sulfuric acid; sodium methylate; In methanol;
DOI:10.1248/cpb.31.698
Post RFQ for Price