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(1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol

Base Information Edit
  • Chemical Name:(1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol
  • CAS No.:509-88-6
  • Molecular Formula:C16H17NO4
  • Molecular Weight:287.3105
  • Hs Code.:
  • Mol file:509-88-6.mol
(1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol

Synonyms:

Suppliers and Price of (1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol
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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 (1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol Edit
Chemical Property:
  • Vapor Pressure:1.97E-10mmHg at 25°C 
  • Boiling Point:490.4°Cat760mmHg 
  • Flash Point:250.4°C 
  • PSA:54.46000 
  • Density:1.56g/cm3 
  • LogP:0.71090 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

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Technology Process of (1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol

There total 4 articles about (1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol 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:

Reference yield: 60.0%

Guidance literature:
C16H17NO4; With triphenylphosphine; benzoic acid; diethylazodicarboxylate; In tetrahydrofuran; at 80 ℃; for 5h;
With lithium aluminium tetrahydride; In tetrahydrofuran; for 0.5h;
DOI:10.1039/c7sc02112g
Guidance literature:
Multi-step reaction with 3 steps
1.1: C40H43ClIrN2P; potassium tert-butylate; hydrogen / ethanol / 0.5 h / 760.05 Torr
2.1: trifluoroacetic acid; dihydrogen peroxide; trichloroacetonitrile / dichloromethane; water / 48 h
3.1: triphenylphosphine; diethylazodicarboxylate; benzoic acid / tetrahydrofuran / 5 h / 80 °C
3.2: 0.5 h
With C40H43ClIrN2P; potassium tert-butylate; hydrogen; dihydrogen peroxide; trichloroacetonitrile; triphenylphosphine; benzoic acid; trifluoroacetic acid; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1039/c7sc02112g

Reference yield:

Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydroxide; water / methanol; tetrahydrofuran
2.1: trifluoroacetic acid; dihydrogen peroxide; trichloroacetonitrile / dichloromethane; water / 48 h
3.1: triphenylphosphine; diethylazodicarboxylate; benzoic acid / tetrahydrofuran / 5 h / 80 °C
3.2: 0.5 h
With water; dihydrogen peroxide; trichloroacetonitrile; triphenylphosphine; benzoic acid; trifluoroacetic acid; sodium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1039/c7sc02112g
upstream raw materials:

(+/-)-oxo-crinine

(-)-epicrinine

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