(4-(Furan-2-yl)phenyl) methanol

Qhov sib xyaw no feem ntau tau txais los ua daj daj kom tawm -dawb crystalline hmoov ntawm ambient kub. Nws cov mis molecular yog C11H10O2, sib xws rau qhov hnyav molecular ntawm 174.20. Lub melting point feem ntau ntog nyob rau hauv thaj tsam ntawm 85–86℃. Qhov ntsuas kub tau kwv yees kwv yees li 310℃ntawm atmospheric siab, suav nrog qhov ceev ze ntawm 1.2 g / cm³. Nws nthuav tawm lipophilicity nruab nrab thiab muaj ib tus neeg pub nyiaj hydrogen (cov pab pawg hydroxyl) thiab ob tus neeg txais nyiaj hydrogen (cov furan oxygen thiab hydroxyl oxygen). Lub compound yog soluble nyob rau hauv cov organic solvents thiab yog ruaj khov nyob rau hauv ib txwm cia tej yam kev mob thaum khaws cia nyob rau hauv ib tug txias, qhuav qhov chaw. Cov qauv kev nyab xeeb kev faib tawm qhia tias muaj peev xwm ua rau tawv nqaij thiab qhov muag khaus thiab ua pa ua pa.

(4-(Furan-2-yl)phenyl)methanol yog biaryl compound uas muaj lub nplhaib phenyl thiab lub nplhaib furan txuas nrog ncaj qha carbon-carbon daim ntawv cog lus, nrog thawj pawg cawv txuas nrog lub nplhaib phenyl. Cov molecule nta ob lub cev muaj ntxhiab tsw: ib qho hluav taws xob nplua nuj furan heterocycle thiab lub nplhaib phenyl, txuas ntawm para txoj hauj lwm txheeb ze rau benzylic cawv. Lub furan oxygen tuaj yeem koom nrog hauv hydrogen bonding lossis hlau sib koom tes, thaum lub benzylic hydroxyl muab ntau qhov chaw rau kev ua haujlwm ntxiv los ntawm oxidation, esterification, lossis etherification. Cov qauv nruj, cov qauv qauv qhia cov khoom siv hluav taws xob tshwj xeeb thiab cov khoom siv tsis zoo, ua rau nws muaj txiaj ntsig zoo rau kev tsim cov txheej txheem molecular ntau dua hauv cov organic synthesis thiab tshuaj chemistry.

Pharmaceutical Intermediate
Cov tshuaj no yog siv los ua ib lub tsev thaiv nyob rau hauv lub synthesis ntawm biologically active molecules. Nws tau raug tshawb xyuas rau nws cov teebmeem cytotoxic tiv thaiv kab mob qog noj ntshav thiab cov furan moiety cuam tshuam nrog kev tiv thaiv -cov khoom siv, ua rau nws muaj feem cuam tshuam rau kev tshawb fawb pharmacological tsom rau kev txhim kho tshuaj.

Enzyme Inhibition Research
Nws tau raug tshawb nrhiav rau nws lub peev xwm los tiv thaiv cov piam thaj-6-phosphate dehydrogenase, ib qho enzyme koom nrog hauv txoj kev pentose phosphate. Qhov kev tiv thaiv no yog kev kho mob txaus siab rau kev kho cov kab mob cab xws li trypanosomiasis, thiab tseem muaj feem cuam tshuam rau kev mob ntshav qab zib thiab mob qog noj ntshav tshawb fawb.

Material Science thiab Organic Synthesis
Raws li ib tug functionalized aromatic molecule, nws ua hauj lwm raws li ib tug intermediate nyob rau hauv lub synthesis ntawm complex organic tebchaw. Nws cov qauv tsim tso cai rau nws siv los tsim cov ntaub ntawv tshiab thiab ua ib qho scaffold hauv tshuaj lom neeg biology rau kev kawm txog kev sib cuam tshuam ntawm molecular.

Flavor thiab Fragrance Applications
Vim nws cov aromatic profile combining furan thiab phenyl pawg, cov compound no kuj raug suav hais tias yog siv los ua tus neeg sawv cev flavoring hauv kev lag luam zaub mov, pab txhawb cov yam ntxwv olfactory rau formulations.

Cim npe nrov: Tuam Tshoj (4-(furan-2-yl)phenyl) methanol manufacturers, lwm tus neeg