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Campestanyl ferulate

Base Information
  • Chemical Name:Campestanyl ferulate
  • CAS No.:106774-77-0
  • Molecular Formula:C38H58O4
  • Molecular Weight:578.876
  • Hs Code.:
  • UNII:GID12I848G
  • ChEMBL ID:CHEMBL3799176
  • Metabolomics Workbench ID:133222
  • Nikkaji Number:J1.610.280F,J1.865.524A
  • Wikidata:Q27279117
Campestanyl ferulate

Synonyms:campestanyl ferulate;trans-Feruloylcampestanol;Campestanol trans-ferulate;trans-Campestanyl ferulate;UNII-GID12I848G;GID12I848G;106774-77-0;Ergostan-3-ol, 3-((2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate), (3beta,5alpha,24R)-;CHEMBL3799176;Q27279117;ERGOSTAN-3-OL, 3-((2E)-3-(4-HYDROXY-3-METHOXYPHENYL)-2-PROPENOATE), (3.BETA.,5.ALPHA.,24R)-

Suppliers and Price of Campestanyl ferulate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of Campestanyl ferulate
Chemical Property:
  • XLogP3:11.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:10
  • Exact Mass:578.43351033
  • Heavy Atom Count:42
  • Complexity:943
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)C)C
  • Isomeric SMILES:C[C@H](CC[C@@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(CC[C@@H](C4)OC(=O)/C=C/C5=CC(=C(C=C5)O)OC)C)C
Technology Process of Campestanyl ferulate

There total 1 articles about Campestanyl ferulate 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:
Multi-step reaction with 2 steps
1: 17 mg / CHCl3 / 2 h / Irradiation
2: 8 mg / pyridine / 10 h / Ambient temperature
With pyridine; In chloroform;
DOI:10.1248/cpb.36.3147
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