Furfuryl glycidyl ether
Product Information
Molecular Formula
C8H10O3
Molecular Weight
154.16
Description
Furfuryl glycidyl ether is an indispensable biomedical chemical that triumphs as a paramount therapeutic entity relentlessly combating sundry afflictions. Its paramount efficacy resides in its role as a reactive diluent, adorning the tapestry of epoxy resin synthesis. Pillars of medicine, epoxy resins empower drug transportation apparatuses, surgical marvels, and the realm of medical contrivances. Moreover, this compound escorts the pharmaceutical realm on its quest for conquering cancer, cardiovascular vicissitudes, and enigmas extant within the neurological domain.
Synonyms
FURFURYL GLYCIDYL ETHER; AKOS NCG-0070; 2,3-EPOXYPROPYL FURFURYL ETHER; 2-[(OXIRANYLMETHOXY)METHYL]FURAN; 2-((2,3-epoxypropoxy)methyl)-fura; 2-((2,3-epoxypropoxy)methyl)furan; 2-((oxiranylmethoxy)methyl)-fura; FURFURYL GLYCIDYL ETHER 98%
IUPAC Name
2-(oxiran-2-ylmethoxymethyl)furan
SMILES
C1C(O1)COCC2=CC=CO2
InChI
InChI=1S/C8H10O3/c1-2-7(10-3-1)4-9-5-8-6-11-8/h1-3,8H,4-6H2
InChI Key
RUGWIVARLJMKDM-UHFFFAOYSA-N
Boiling Point
103-104°C (11 mmHg)
Flash Point
215.6 °CF - closed cup
Purity
98%
Density
1.122
Appearance
Colorless transparent liquid
Refractive Index
n20/D 1.481 (lit.)
QC Data
Computed Properties
XLogP3
0.4
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
4
Exact Mass
154.062994177 g/mol
Monoisotopic Mass
154.062994177 g/mol
Topological Polar Surface Area
34.9Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
127
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
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 |
|---|---|---|
| RU-2756806-C1 | Low-viscosity epoxy binder for reinforced plastics with high crack resistance and heat resistance | 2020-12-26 |
| US-2022064505-A1 | One-component thermosetting epoxy adhesive with improved adhesion | 2020-08-31 |
| CN-111848924-A | Synthetic method and application of low-viscosity fluorine-containing hyperbranched polyether type epoxy resin | 2020-08-25 |
| CN-111944120-A | Preparation method and application of low-viscosity polyether type hyperbranched epoxy resin | 2020-08-25 |
| CN-111944120-B | Preparation method and application of low-viscosity polyether type hyperbranched epoxy resin | 2020-08-25 |
| WO-2022046560-A1 | Fluorescent dye loaded polymeric taggants for depth determination in drilling wells | 2020-08-24 |
| WO-2022038297-A1 | Self-healing polymers | 2020-08-21 |
| WO-2022008919-A1 | Polymerisation process | 2020-07-08 |
| WO-2021251099-A1 | Easily disintegrable adhesive material, article and disintegration method | 2020-06-12 |
| CN-111574820-A | Self-repairing cross-linked polyurethane and preparation method thereof | 2020-04-24 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 11858762 | 2002-02-01 | Choosing the best pulse sequences, acquisition parameters, postacquisition processing strategies, and probes for natural product structure elucidation by NMR spectroscopy | Journal of natural products |
