5-(Ethoxymethyl)furan-2-carboxaldehyde - CAS 1917-65-3
Catalog: |
BB014836 |
Product Name: |
5-(Ethoxymethyl)furan-2-carboxaldehyde |
CAS: |
1917-65-3 |
Synonyms: |
5-(ethoxymethyl)furan-2-carbaldehyde |
IUPAC Name: | 5-(ethoxymethyl)furan-2-carbaldehyde |
Description: | 5-(Ethoxymethyl)furan-2-carboxaldehyde (CAS# 1917-65-3) is a useful research chemical compound. |
Molecular Weight: | 154.16 |
Molecular Formula: | C8H10O3 |
Canonical SMILES: | CCOCC1=CC=C(O1)C=O |
InChI: | InChI=1S/C8H10O3/c1-2-10-6-8-4-3-7(5-9)11-8/h3-5H,2,6H2,1H3 |
InChI Key: | CCDRPZFMDMKZSZ-UHFFFAOYSA-N |
Boiling Point: | 234.258 °C at 760 mmHg |
Density: | 1.104 g/cm3 |
Appearance: | Liquid |
MDL: | MFCD06803262 |
LogP: | 1.62860 |
GHS Hazard Statement: | H318 (100%): Causes serious eye damage [Danger Serious eye damage/eye irritation]; H411 (100%): Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard] |
Precautionary Statement: | P264+P265, P273, P280, P305+P354+P338, P317, P391, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-112898246-A | Method for preparing 5-ethoxy methyl furfural | 20210120 |
CN-112830916-A | Preparation method of 2, 5-furandicarboxylic acid under mild condition | 20200702 |
CN-112830916-B | Preparation method of 2, 5-furandicarboxylic acid under mild condition | 20200702 |
CN-111389395-A | Ruthenium iridium catalyst, preparation method thereof and application of ruthenium iridium catalyst in hydrogenolysis reaction of 5-hydroxymethylfurfural | 20200506 |
CN-111266135-A | Multifunctional acid catalyst and preparation method and application thereof | 20200219 |
PMID | Publication Date | Title | Journal |
22639414 | 20120901 | One-pot conversions of lignocellulosic and algal biomass into liquid fuels | ChemSusChem |
22749371 | 20120901 | Catalytic selective etherification of hydroxyl groups in 5-hydroxymethylfurfural over H4SiW12O40/MCM-41 nanospheres for liquid fuel production | Bioresource technology |
22609675 | 20120701 | Conversion of glucose into furans in the presence of AlCl3 in an ethanol-water solvent system | Bioresource technology |
22264628 | 20120301 | Conversion of fructose into 5-hydroxymethylfurfural (HMF) and its derivatives promoted by inorganic salt in alcohol | Carbohydrate research |
22004121 | 20111124 | Theoretical studies on thermochemistry for conversion of 5-chloromethylfurfural into valuable chemicals | The journal of physical chemistry. A |
Complexity: | 125 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 154.062994177 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 154.062994177 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 39.4 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.3 |
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