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5-O-mycaminosylprotylonolide

Base Information
  • Chemical Name:5-O-mycaminosylprotylonolide
  • CAS No.:81661-90-7
  • Molecular Formula:C31H53NO8
  • Molecular Weight:567.764
  • Hs Code.:
  • Mol file:81661-90-7.mol
5-O-mycaminosylprotylonolide

Synonyms:5-O-mycaminosyl tylactone;(11Z,13E)-6-[4-(dimethylamino)-3,5-dihydroxy-6-methyloxan-2-yl]oxy-7,16-diethyl-4-hydroxy-5,9,13,15-tetramethyl-1-oxacyclohexadeca-11,13-diene-2,10-dione;mycaminosyl tylactone;5-O-Mycaminosylprotylonolide;5-Mcpt;5-O-beta-D-mycaminosyltylactone;

Suppliers and Price of 5-O-mycaminosylprotylonolide
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 4 raw suppliers
Chemical Property of 5-O-mycaminosylprotylonolide
Chemical Property:
  • Vapor Pressure:1.69E-24mmHg at 25°C 
  • Boiling Point:728.4°C at 760 mmHg 
  • Flash Point:394.3°C 
  • PSA:125.76000 
  • Density:1.13g/cm3 
  • LogP:3.25100 
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 5-O-mycaminosylprotylonolide

There total 6 articles about 5-O-mycaminosylprotylonolide 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 sodium cyanoborohydride; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 50 ℃; for 8.5h;
DOI:10.1248/cpb.30.97
Guidance literature:
Multi-step reaction with 5 steps
1: 0.2N HCl / 4 h
2: 6.5 g / 0.5N HCl / 20 h / 90 °C
3: 3.0 g / NaBH4, 0.2 M phosphate buffer / methanol / 19 h / Ambient temperature
4: 2.1 g / I2, triphenylphosphine / dimethylformamide / 2 h / Ambient temperature
5: 1.2 g / NaBH3CN / hexamethylphosphoric acid triamide / 8.5 h / 50 °C
With hydrogenchloride; sodium tetrahydroborate; phosphate buffer; iodine; sodium cyanoborohydride; triphenylphosphine; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; N,N-dimethyl-formamide;
DOI:10.1248/cpb.30.97
Guidance literature:
Multi-step reaction with 2 steps
1: 2.1 g / I2, triphenylphosphine / dimethylformamide / 2 h / Ambient temperature
2: 1.2 g / NaBH3CN / hexamethylphosphoric acid triamide / 8.5 h / 50 °C
With iodine; sodium cyanoborohydride; triphenylphosphine; In N,N,N,N,N,N-hexamethylphosphoric triamide; N,N-dimethyl-formamide;
DOI:10.1248/cpb.30.97
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