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delta7-Avenasterol

Base Information
  • Chemical Name:delta7-Avenasterol
  • CAS No.:23290-26-8
  • Molecular Formula:C29H48O
  • Molecular Weight:412.7
  • Hs Code.:
  • UNII:I0WYR6393O
  • Metabolomics Workbench ID:34972
  • Nikkaji Number:J451.682F,J83.540D,J794.504C
  • Wikidata:Q76422902
  • Wikipedia:Avenasterol
delta7-Avenasterol

Synonyms:delta7-Avenasterol;avenasterol;23290-26-8;24Z-Ethylidenelathosterol;I0WYR6393O;Z-24-Ethylidene-5alpha-cholest-7-en-3beta-ol;24Z-ethylidene-cholest-7-en-3beta-ol;Stigmasta-7,24(28)-dien-3-ol, (3beta,5alpha,24Z)-;(3S,5S,9R,10S,13R,14R,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol;7212-91-1;(3S,5S,9R,10S,13R,14R,17R)-17-((R)-5-Isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol;7-Dehydroavenasterol;UNII-I0WYR6393O;Stigmasta-7,24(28)-dien-3-ol, (3b,5a,24Z)-;AVENASTEROL, DELTA7;AVENASTEROL, .DELTA.7;big up tri, open7-Avenasterol;LMST01040154;AKOS027326804;5alpha-Stigmasta-7,24(28)-dien-3-ol;1ST000356;HY-107210;5alpha-Stigmasta-7,24(28)-dien-3beta-ol;CS-0027649;5alpha-Stigmasta-7,Z-24(28)-diene-3.beta-ol;(Z)-5alpha-Stigmasta-7,24(28)-dien-3beta-ol;3beta-Hydroxy-5alpha-stigmasta-7,24(28)Z-diene;(24z)-24-ethylidene-5alpha-cholest-7-en-3beta-ol;(24Z)-5alpha-Stigmasta-7,24(28)-dien-3beta-ol;(24Z)-24-Ethyl-5alpha-cholesta-7,24(28)-dien-3beta-ol;Z-24-ETHYLIDENE-5.ALPHA.-CHOLEST-7-EN-3.BETA.-OL;(3S, 5S, 9R, 10S, 13R, 14R, 17R)-10, 13-dimethyl-17-[(Z, 2R)-5-propan-2-ylhept-5-en-2-yl]-2, 3, 4, 5, 6, 9, 11, 12, 14, 15, 16, 17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol;(3S,5S,9R,10S,13R,14R,17R)-17-((R,Z)-5-Isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

Suppliers and Price of delta7-Avenasterol
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
  • Δ7-Avenasterol(E/Zmixture)
  • 5mg
  • $ 1620.00
  • Biosynth Carbosynth
  • Delta 7-avenasterol
  • 1 mg
  • $ 500.00
  • Biosynth Carbosynth
  • Delta 7-avenasterol
  • 500 ug
  • $ 400.00
  • Biosynth Carbosynth
  • Delta 7-avenasterol
  • 250 ug
  • $ 300.00
  • Biosynth Carbosynth
  • Delta 7-avenasterol
  • 5 mg
  • $ 1000.00
  • Biosynth Carbosynth
  • Delta 7-avenasterol
  • 2 mg
  • $ 800.00
  • Arctom
  • Delta7-avenasterol ≥98%
  • 5mg
  • $ 595.00
Total 19 raw suppliers
Chemical Property of delta7-Avenasterol
Chemical Property:
  • Boiling Point:503.1±49.0 °C(Predicted) 
  • PKA:15.10±0.70(Predicted) 
  • PSA:20.23000 
  • Density:0.98±0.1 g/cm3(Predicted) 
  • LogP:7.94490 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • XLogP3:8.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:5
  • Exact Mass:412.370516150
  • Heavy Atom Count:30
  • Complexity:687
Purity/Quality:

99% *data from raw suppliers

Δ7-Avenasterol(E/Zmixture) *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C
  • Isomeric SMILES:C/C=C(/CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C)\C(C)C
  • Uses Δ7-Avenasterol is an analog of Stigmasterol (S686750); a plant sterol that is used as a precursor in the synthesis of progesterone.
Technology Process of delta7-Avenasterol

There total 2 articles about delta7-Avenasterol 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:
(24(28)Z)-Δ7,24(28)-5α-3β-acetoxy-stigmastadien, K2CO3;
Guidance literature:
(24(28)Z)-Δ7,24(28)-5α-3β-acetoxy-stigmastadien, K2CO3;
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