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Tert-butyl 7-hydroxyheptanoate

Base Information
  • Chemical Name:Tert-butyl 7-hydroxyheptanoate
  • CAS No.:86013-78-7
  • Molecular Formula:C11H22O3
  • Molecular Weight:202.294
  • Hs Code.:
  • European Community (EC) Number:867-701-9
Tert-butyl 7-hydroxyheptanoate

Synonyms:tert-butyl 7-hydroxyheptanoate;86013-78-7;tert-Butyl7-Hydroxyheptanoate;starbld0007384;SCHEMBL8507410;AT11173;BP-28093;BS-48287;EN300-138042

Suppliers and Price of Tert-butyl 7-hydroxyheptanoate
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 6 raw suppliers
Chemical Property of Tert-butyl 7-hydroxyheptanoate
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:8
  • Exact Mass:202.15689456
  • Heavy Atom Count:14
  • Complexity:158
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)CCCCCCO
Technology Process of Tert-butyl 7-hydroxyheptanoate

There total 3 articles about Tert-butyl 7-hydroxyheptanoate 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 dimethylsulfide borane complex; In tetrahydrofuran; at 0 - 20 ℃; for 24h;
Guidance literature:
With di-tert-butyl peroxide; potassium iodide; at 130 ℃; for 8h; Sealed tube; Green chemistry;
DOI:10.1039/c7gc03745g
Guidance literature:
Multi-step reaction with 2 steps
1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 18 h / 20 °C
2: dimethylsulfide borane complex / tetrahydrofuran / 24 h / 0 - 20 °C
With dmap; dimethylsulfide borane complex; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane;
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