Bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic Anhydride
Product Information
Molecular Formula
C10H10O3
Molecular Weight
178.18
Description
Bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride is a useful research chemical.
Synonyms
4-oxatricyclo[5.2.2.0^{2,6}]undec-8-ene-3,5-dione; 4-oxatricyclo[5.2.2.0^{2,6}]undec-8-ene-3,5-dione
IUPAC Name
4-oxatricyclo[5.2.2.02,6]undec-8-ene-3,5-dione
SMILES
C1CC2C=CC1C3C2C(=O)OC3=O
InChI
InChI=1S/C10H10O3/c11-9-7-5-1-2-6(4-3-5)8(7)10(12)13-9/h1-2,5-8H,3-4H2
InChI Key
YIHKILSPWGDWPR-UHFFFAOYSA-N
Boiling Point
340.9±42.0 °C (Predicted)
Melting Point
148 °C
Density
1.324 g/cm3
Solubility
Other solvents(Soluble) : Acetone
LogP
0.89820
Safety Information
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning
Computed Properties
XLogP3
1.2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
0
Exact Mass
178.062994177 g/mol
Monoisotopic Mass
178.062994177 g/mol
Topological Polar Surface Area
43.4Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
288
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
4
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-114058008-A | Process for preparing semi-aromatic polyamides end-capped with monocarboxylic acids, semi-aromatic polyamides and molding compositions | 2021-12-13 |
| CN-114058009-A | Process for preparing semi-aromatic polyamides with reduced loss of diamine monomer, semi-aromatic polyamides and molding compositions | 2021-12-13 |
| CN-114058010-A | Process for preparing low-energy semiaromatic polyamides, semiaromatic polyamides and moulding compositions | 2021-12-13 |
| CN-114133559-A | Process for preparing semiaromatic polyamides with reduced salt formation cycle, semiaromatic polyamides and moulding compositions | 2021-12-13 |
| CN-114133560-A | Process for preparing semiaromatic polyamides with improved impact strength, semiaromatic polyamides and moulding compositions | 2021-12-13 |
| CN-113321970-A | White inkjet ink compositions having improved resin compatibility | 2021-01-05 |
| CN-114181391-A | Thermoplastic polyimide resin and preparation method thereof | 2020-09-14 |
| CN-114181528-A | Thermoplastic polyimide composition and application thereof, and preparation and application of thermoplastic polyimide | 2020-09-14 |
| JP-2022022496-A | Measurement method and measurement reagent for carboxy group-containing water-soluble polymer concentration | 2020-06-24 |
| JP-2021195451-A | Epoxy resin composition | 2020-06-15 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 11724614 | 2001-12-05 | NMR experimental evidence of the differentiation of enantiotopic directions in C(s) and C(2v) molecules using partially oriented, chiral media | Journal of the American Chemical Society |
