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Tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate

Base Information
  • Chemical Name:Tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate
  • CAS No.:797038-33-6
  • Molecular Formula:C9H16O4
  • Molecular Weight:188.224
  • Hs Code.:
  • DSSTox Substance ID:DTXSID801198791
Tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate

Synonyms:tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate;797038-33-6;Tert-butyl 4-hydroxyoxolane-3-carboxylate;t-butyl 4-hydroxytetrahydrofuran-3-carboxylate;SCHEMBL1267055;KSFWORQWMLHPPN-UHFFFAOYSA-N;DTXSID801198791;MFCD28363986;AKOS034831980;LS-11430;FT-0754495;W19594;1,1-Dimethylethyl tetrahydro-4-hydroxy-3-furancarboxylate

Suppliers and Price of Tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate
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
  • Matrix Scientific
  • tert-Butyl 4-hydroxytetrahydrofuran-3-carboxylate
  • 5g
  • $ 2200.00
  • Matrix Scientific
  • tert-Butyl 4-hydroxytetrahydrofuran-3-carboxylate
  • 1g
  • $ 600.00
  • Matrix Scientific
  • tert-Butyl 4-hydroxytetrahydrofuran-3-carboxylate
  • 0.500g
  • $ 480.00
Total 1 raw suppliers
Chemical Property of Tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate
Chemical Property:
  • Boiling Point:274.8±40.0 °C(Predicted) 
  • Density:1.148±0.06 g/cm3(Predicted) 
  • XLogP3:0.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:188.10485899
  • Heavy Atom Count:13
  • Complexity:194
Purity/Quality:

tert-Butyl 4-hydroxytetrahydrofuran-3-carboxylate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)C1COCC1O
Technology Process of Tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate

There total 3 articles about Tert-butyl 4-hydroxytetrahydrofuran-3-carboxylate 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 tetrahydroborate; In isopropyl alcohol; at 0 - 20 ℃;
DOI:10.1039/b407558g
Guidance literature:
Multi-step reaction with 2 steps
1.1: NaH / diethyl ether / 0.5 h / 20 °C
1.2: 68 percent / dimethylsulfoxide / 0.5 h / 20 °C
2.1: 89 percent / NaBH4 / propan-2-ol / 0 - 20 °C
With sodium tetrahydroborate; sodium hydride; In diethyl ether; isopropyl alcohol;
DOI:10.1039/b407558g
Guidance literature:
Multi-step reaction with 2 steps
1.1: sodium hydride / diethyl ether / 0.5 h / 20 °C / Inert atmosphere
1.2: 0.5 h / 0 - 20 °C
2.1: sodium tetrahydroborate / isopropyl alcohol / 0 - 20 °C
With sodium tetrahydroborate; sodium hydride; In diethyl ether; isopropyl alcohol;
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