Home Other Building Blocks 3-Oxotetrahydrofuran

3-Oxotetrahydrofuran

CAS No.:
22929-52-8
Catalog Number:
AG002LJ3
Molecular Formula:
C4H6O2
Molecular Weight:
86.0892
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$22
- +
25g
95%
In Stock USA
United States
$67
- +
100g
95%
In Stock USA
United States
$167
- +
Product Description
Catalog Number:
AG002LJ3
Chemical Name:
3-Oxotetrahydrofuran
CAS Number:
22929-52-8
Molecular Formula:
C4H6O2
Molecular Weight:
86.0892
MDL Number:
MFCD07778393
IUPAC Name:
oxolan-3-one
InChI:
InChI=1S/C4H6O2/c5-4-1-2-6-3-4/h1-3H2
InChI Key:
JLPJFSCQKHRSQR-UHFFFAOYSA-N
SMILES:
O=C1COCC1
Properties
Complexity:
67.9  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
86.037g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
86.09g/mol
Monoisotopic Mass:
86.037g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.4  
Literature
Title Journal
Stereoselective synthesis of donor-acceptor substituted cyclopropafuranones by intramolecular cyclopropanation of vinylogous carbonates: divergent synthesis of tetrahydrofuran-3-one, tetrahydropyran-3-one, and lactones. Organic letters 20091203
Caryophyllenes from a fungal culture of Chrysosporium pilosum. Journal of natural products 20090327
Singlet-oxygen-mediated one-pot synthesis of 3-keto-tetrahydrofurans from 2-(beta-hydroxyalkyl) furans. Organic letters 20090115
Antiplasmodial hirsutinolides from Vernonia staehelinoides and their utilization towards a simplified pharmacophore. Phytochemistry 20070401
Structure-activity studies of cyclic ketone inhibitors of the serine protease plasmin: design, synthesis, and biological activity. Bioorganic & medicinal chemistry 20061215
Modeling deoxyribose radicals by neutralization-reionization mass spectrometry. Part 2. Preparation, dissociations, and energetics of 3-hydroxyoxolan-3-yl radical and cation. Journal of the American Society for Mass Spectrometry 20040701
Enantioselective total syntheses of slagenins A-C and their antipodes. The Journal of organic chemistry 20030321
Properties