Chemical Properties of 2,5-Furandione, dihydro- (CAS 108-30-5)

2,5-Furandione, dihydro-

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InChI
InChI=1S/C4H4O3/c5-3-1-2-4(6)7-3/h1-2H2
InChI Key
RINCXYDBBGOEEQ-UHFFFAOYSA-N
Formula
C4H4O3
SMILES
O=C1CCC(=O)O1
Molecular Weight1
100.07
CAS
108-30-5
Other Names
  • 2,5(3H,4H)-Furandione
  • 2,5-Diketotetrahydrofuran
  • 2,5-Dioxotetrahydrofuran
  • 2,5-Furandione, dihydro-
  • Bernsteinsaure-anhydrid
  • Butanedioic anhydride
  • Dihydro-2,5-diketotetrahydrofuran
  • Dihydro-2,5-furandione
  • NCI-C55696
  • NSC 8518
  • Rikacid SA
  • Succinic acid anhydride
  • Succinyl anhydride
  • Succinyl oxide
  • Tetrahydro-2,5-dioxofuran
  • Tetrahydro-2,5-furandione
Sources

Physical Properties

Property Value Unit Source
Δcsolid -1537.10 ± 0.40 kJ/mol NIST
Δcsolid -1543.90 ± 0.63 kJ/mol NIST
Δf -304.24 kJ/mol Joback Calculated Property
Δfgas -527.90 ± 1.70 kJ/mol NIST
Δfsolid -608.60 ± 0.70 kJ/mol NIST
Δfus 5.98 kJ/mol Joback Calculated Property
Δsub 80.70 ± 1.60 kJ/mol NIST
Δsub 80.70 ± 1.60 kJ/mol NIST
Δsub 80.70 kJ/mol NIST
Δvap 38.07 kJ/mol Joback Calculated Property
IE [10.80; 10.84] eV Show Hide
IE 10.84 eV NIST
IE 10.84 eV NIST
IE 10.84 eV NIST
IE 10.80 eV NIST
logPoct/wat -0.15 Crippen Calculated Property
Pc 5670.27 kPa Joback Calculated Property
Tboil 534.20 K NIST
Tc 717.29 K Joback Calculated Property
Tfus 392.60 ± 1.00 K NIST
Tfus 393.15 ± 1.50 K NIST
Tfus 392.00 ± 1.00 K NIST
Vc 0.24 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 133.07 J/mol×K 473.46 Joback Calculated Property
ΔsubH 82.20 kJ/mol 300.5 NIST
ΔsubH 80.50 ± 1.60 kJ/mol 309.0 NIST
ΔvapH 57.30 kJ/mol 467.5 NIST

Molecular Descriptors

Joback and Reid Groups
-O- (ring) 1
>C=O (ring) 2
-CH2- (ring) 2

Similar Compounds

Butyrolactone. Oxolan-2-one. Acetic propanoic anhydride. Succinaldehydic acid, methyl ester. Butanoic acid, anhydride. Butanoic acid, ethyl ester. Propanoic acid, anhydride. Butanoic acid, propyl ester. Butanoic acid, methyl ester. Butanoic acid, butyl ester. ethyl 4-hydroxybutanoate. Propanoic acid, ethyl ester. 2(3H)-Furanone, dihydro-4-methyl-. (S)-dihydro-4-methylfuran-2(3H)-one. 2H-Pyran-2,6(3H)-dione, dihydro-.

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