furfuryl


Also found in: Medical.

furfuryl

[′fər·fə‚ril]
(organic chemistry)
The functional group C5H6O‒ from furfural.
References in periodicals archive ?
Epichlorohydrin, glycidyl furfuryl ether, 1,1'methylenedi-4,1-phenylene-bismaleimmide, 4,4'-diaminodiphenylmethane (DDM), O,O'-bis(2-aminopropyl) polypropylene glycol-block-polyethylene glycol-block-polypropylene glycol (Jeff 500), chloroform, acetonitrile, sodium hydroxide were purchased from Sigma Aldrich and used as received.
For instance, the advanced inorganic binders commercialized for aluminum automotive applications and reductions in monomer content in traditional organic binders reduced "free" furfuryl alcohol in furan nobake binders and free phenol content in urethane cold-box binders.
In the degradation process, furfural is converted into furfuryl alcohol, and due to the similar structure of HMF and furfural, the conversion of HMF into 2.
The volatile esters were lower, whereas some compounds typical of oxidized wines increased, such as 1,1,6-trimethyl-1,2-dihydronaphthalene, furfuryl ether.
Surface modification of coir fibre involving oxidation of lignins followed by reaction with furfuryl alcohol: Characterization and stability.
Emergence of novel furfural application to manufacture THF, furfuryl alcohol resins and furanics is also expected to have a positive influence on the market growth.
Key statement: The present invention is directed to a pneumatic tire comprising a component, the component comprising a rubber composition comprising a diene based elastomer and 1 to 100 phr of: A) a twin polymerization reaction product of a silyl ether; or B) a twin polymerization reaction product of a boronic acid ester; or C) a twin polymerization reaction product of a titanium compound derived from tetraethyl orthotitanate and furfuryl alcohol; or D) a twin polymerization reaction product of a tungsten compound.
Enzymatic studies in the metabolism of the tetrahydro furfuryl mercaptan moiety of thiamine tetrahydrofurfuryl disulfide.
Compounds with methoxy and hetero furfuryl substituent at the meta position to the phenyl ring at 2nd position and at the 2nd position to the imidazole ring of the compound X2 and Z8 led to considerable increase in the activity.
Bart Vanderhaegen of Katholieke Universiteit Leuven in Heverlee, Belgium, and his colleagues have discovered that furfuryl ethyl ether contributes an unpleasant "solvent" or "chemical" flavor with age, primarily in ales.
Alternatively, furfuryl alcohol can be used as the removal solvent.
They used these rules as well as mathematical algorithms to predict bow detoxification pathways would metabolize ethyl and furfuryl alcohol.