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10-(acetyloxy)-4,6,9-trimethyl-13-methylidene-12-oxodecahydro-2H-2,9-pentanofuro[2,3,4-ef][3]benzoxepin-3-yl butanoate

Base Information
  • Chemical Name:10-(acetyloxy)-4,6,9-trimethyl-13-methylidene-12-oxodecahydro-2H-2,9-pentanofuro[2,3,4-ef][3]benzoxepin-3-yl butanoate
  • CAS No.:74145-71-4
  • Molecular Formula:C26H38O7
  • Molecular Weight:462.584
  • Hs Code.:
10-(acetyloxy)-4,6,9-trimethyl-13-methylidene-12-oxodecahydro-2H-2,9-pentanofuro[2,3,4-ef][3]benzoxepin-3-yl butanoate

Synonyms:

Suppliers and Price of 10-(acetyloxy)-4,6,9-trimethyl-13-methylidene-12-oxodecahydro-2H-2,9-pentanofuro[2,3,4-ef][3]benzoxepin-3-yl butanoate
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Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 10-(acetyloxy)-4,6,9-trimethyl-13-methylidene-12-oxodecahydro-2H-2,9-pentanofuro[2,3,4-ef][3]benzoxepin-3-yl butanoate
Chemical Property:
  • Vapor Pressure:3.49E-12mmHg at 25°C 
  • Boiling Point:550.9°Cat760mmHg 
  • Flash Point:233.8°C 
  • Density:1.17g/cm3 
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 10-(acetyloxy)-4,6,9-trimethyl-13-methylidene-12-oxodecahydro-2H-2,9-pentanofuro[2,3,4-ef][3]benzoxepin-3-yl butanoate

There total 2 articles about 10-(acetyloxy)-4,6,9-trimethyl-13-methylidene-12-oxodecahydro-2H-2,9-pentanofuro[2,3,4-ef][3]benzoxepin-3-yl butanoate 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 manganese(IV) oxide; In chloroform; for 2h; Ambient temperature;
DOI:10.1021/ja00535a047
Guidance literature:
Multi-step reaction with 3 steps
1: 90 percent / pyridine / 48 h / Ambient temperature
2: 65 percent / O2, methylene blue / CH2Cl2 / 12 h / 0 - 10 °C / Irradiation
3: 80 percent / MnO2 / CHCl3 / 2 h / Ambient temperature
With pyridine; manganese(IV) oxide; oxygen; methylene blue; In dichloromethane; chloroform;
DOI:10.1021/ja00535a047
Guidance literature:
Multi-step reaction with 2 steps
1: 70 percent / LiAlH4 / diethyl ether / 0.5 h / -78 °C
2: 53 percent / pyridine / 18 h / Ambient temperature
With lithium aluminium tetrahydride; In pyridine; diethyl ether;
DOI:10.1021/jo00318a023
upstream raw materials:

asbestinin-5

asbestinin-3

Downstream raw materials:

asbestinin-5-acetate

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