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(4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol

Base Information
  • Chemical Name:(4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol
  • CAS No.:936324-78-6
  • Molecular Formula:C10H20O2
  • Molecular Weight:172.268
  • Hs Code.:
(4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol

Synonyms:(4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol

Suppliers and Price of (4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol
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 1 raw suppliers
Chemical Property of (4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol

There total 5 articles about (4S,5R)-4-methyl-5-pentyltetrahydro-2-furanol 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 4 steps
1: 70 percent / sodium / diethyl ether / 3 h / 0 °C
2: N-bromosuccinimide / CH2Cl2 / 4 h / 20 °C
3: tri-n-butyl tin hydride / N,N'-azoisobutyronitrile / benzene / 2 h / Heating
4: 2 g / aq. acetic acid / 4 h / Heating
With N-Bromosuccinimide; tri-n-butyl-tin hydride; sodium; acetic acid; 2,2'-azobis(isobutyronitrile); In diethyl ether; dichloromethane; benzene;
DOI:10.1080/00397910601055057
Guidance literature:
Multi-step reaction with 2 steps
1: tri-n-butyl tin hydride / N,N'-azoisobutyronitrile / benzene / 2 h / Heating
2: 2 g / aq. acetic acid / 4 h / Heating
With tri-n-butyl-tin hydride; acetic acid; 2,2'-azobis(isobutyronitrile); In benzene;
DOI:10.1080/00397910601055057
Guidance literature:
Multi-step reaction with 3 steps
1: N-bromosuccinimide / CH2Cl2 / 4 h / 20 °C
2: tri-n-butyl tin hydride / N,N'-azoisobutyronitrile / benzene / 2 h / Heating
3: 2 g / aq. acetic acid / 4 h / Heating
With N-Bromosuccinimide; tri-n-butyl-tin hydride; acetic acid; 2,2'-azobis(isobutyronitrile); In dichloromethane; benzene;
DOI:10.1080/00397910601055057
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