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Nimbanal

Base Information Edit
  • Chemical Name:Nimbanal
  • CAS No.:120462-51-3
  • Molecular Formula:C29H34O8
  • Molecular Weight:510.584
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20557187
  • Nikkaji Number:J3.359.306F
  • Mol file:120462-51-3.mol
Nimbanal

Synonyms:Nimbanal;120462-51-3;methyl 2-[(1S,2R,3S,4R,8R,9S,10R,13R,15R)-2-acetyloxy-4-formyl-13-(furan-3-yl)-4,8,10,12-tetramethyl-7-oxo-16-oxatetracyclo[8.6.0.03,8.011,15]hexadeca-5,11-dien-9-yl]acetate;SCHEMBL22091576;DTXSID20557187;J-004349;Methyl [(2R,3aR,4aS,5R,5aS,9aR,10S,10aR)-5-(acetyloxy)-6-formyl-2-(furan-3-yl)-1,6,9a,10a-tetramethyl-9-oxo-3,3a,4a,5,5a,6,9,9a,10,10a-decahydro-2H-cyclopenta[b]naphtho[2,3-d]furan-10-yl]acetate

Suppliers and Price of Nimbanal
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
  • TRC
  • Nimbanal
  • 25 mg
  • $ 1695.00
Total 1 raw suppliers
Chemical Property of Nimbanal Edit
Chemical Property:
  • Melting Point:>164°C (dec.) 
  • PSA:109.11000 
  • LogP:3.94830 
  • Storage Temp.:Amber Vial, -20°C Freezer, Under inert atmosphere 
  • Solubility.:Chloroform (Slightly) 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:7
  • Exact Mass:510.22536804
  • Heavy Atom Count:37
  • Complexity:1090
Purity/Quality:

98% *data from raw suppliers

Nimbanal *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C2C(CC1C3=COC=C3)OC4C2(C(C5(C(C4OC(=O)C)C(C=CC5=O)(C)C=O)C)CC(=O)OC)C
  • Isomeric SMILES:CC1=C2[C@@H](C[C@H]1C3=COC=C3)O[C@H]4[C@@]2([C@@H]([C@@]5([C@@H]([C@H]4OC(=O)C)[C@](C=CC5=O)(C)C=O)C)CC(=O)OC)C
  • Uses Nimbin (N476280) derivative.
Technology Process of Nimbanal

There total 1 articles about Nimbanal 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 pyridine; dmap; for 18h;
DOI:10.1016/S0040-4020(01)81360-0
upstream raw materials:

6-deacetylnimbinal

acetyl chloride

Refernces Edit
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