(2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone(CAS#17092-92-1)

(2,6,6-Trimethyl-2-hydroxycyclohexylidene)acetic acid lactone(CAS#17092-92-1)

1. Basic Information
Zita: (2,6,6-Trimethyl-2-hydroxycyclohexylidene) acetic acid lactone.
Nhamba yeCAS:17092-92-1, inova nhamba yakasarudzika yekuzivikanwa yekomboni muchemikari yekunyoresa zvinhu, iyo yakanakira kubvunza chaiko uye kutora data pasi rese.
Chechipiri, maitiro ezvimiro
Chimiro chayo chemolecular ine nhanhatu-nhengo cyclohexyl boka ine hydroxyl boka rakanamatira kune iyo 2 chinzvimbo, uye trimethyl inotsiva panzvimbo iyi, iyo inopa molekuru imwe steric chipingamupinyi uye zvemagetsi zvinhu. Kune zvakare chimiro chelactone chakaumbwa neboka remethylene uye carbonyl boka mumorekuru, iro rine kumwe kugadzikana uye rine chekuita kwakakosha pachiitiko chemakemikari, kunyungudika uye zvimwe zvemuviri nemakemikari emukomboni.
3. Zvinhu zvemuviri
Chitarisiko: Kazhinji chena kusvika kuchiedza yellow crystalline poda kana yakasimba, yakagadzikana mamiriro, nyore kuchengeta uye kubata.
Solubility: Iine kumwe kunyungudika mune zvakajairika organic zvinonyungudutsa senge ethanol, ether, chloroform, nezvimwewo, uye inogona kugadzira yunifomu mhinduro yekuzotevera kemikari kana bvunzo dzekuongorora; Iyo ine kunyungudika kwakashata mumvura uye inoteedzera musimboti we "samilar dissolvability", ichiratidza iyo isiri-polar molecular nature.
Melting point: Iyo ine yakatemerwa nzvimbo yekunyunguduka, inova imwe yeakakosha zviratidzo zvekuchena, uye kuchena kwemuenzaniso kunogona kutanga kutongwa nekunyatsoona nzvimbo yekunyungudika, uye iyo chaiyo yekunyungudika kukosha inogona kubvunzwa mukati. nyanzvi dzemakemikari mabhuku kana dhatabhesi.
Chechina, makemikari zvinhu
Iine yakajairika ring-kuvhura uye yakavharwa-loop reactivity ye lactone, uye pasi pemamiriro ezvinhu anokonzera asidi uye alkali, mhete ye lactone inogona kuputsika, uye inopindirana ne nucleophiles uye electrophiles kuti ibudise mutsara wezvinobva, zvichipa zvakasiyana-siyana. nzira dze organic synthesis.
Seboka rinoshanda rinoshanda, boka rehydroxyl rinogona kutora chikamu mu esterification, etherification uye mamwe maitiro kuti awedzere kushandura chimiro chemolecular uye kuwedzera huwandu hwayo hwemashandisirwo, sekugadzirira ester makomisheni ane yakakosha biological chiitiko chekutsvaga zvinodhaka nekusimudzira.
5. Synthesis nzira
Nzira yakajairwa yekugadzira ndeye kushandisa cyclohexanone zvinobva kune zvakafanira zvinotsiva sechinhu chekutanga, uye kuvaka chinongedzo chemolecular chimiro kuburikidza neakawanda-nhanho maitiro. Semuyenzaniso, mapoka etrimethyl anounzwa kuburikidza nealkylation reaction, uyezve mhete dzelactone nemapoka ehydroxyl anovakwa neoxidation uye cyclization, uye maitiro ekuita senge tembiricha, pH, nguva yekuita, nezvimwe zvinoda kunyatsodzorwa mukati mekuita kuti ive nechokwadi. goho rakakwirira uye kuchena.
Yechitanhatu, ndima yekushandisa
Indasitiri yekunhuhwirira: nekuda kwechimiro chayo chakasarudzika inounza kunhuhwirira kwakakosha, inogona kushandiswa sechinhu chinonhuwira muzvinonhuwira, zvizorwa, zvinonhuhwirira zvekudya, nezvimwewo, mushure mekudimburudza uye kusanganisa, kuwedzera yakasarudzika flavour.
Pharmaceutical field: Seyepakati mukugadzirwa kwezvinodhaka, zvimedu zvayo zvechimiro zvinogona kuunzwa mumamorekuru ane pharmacological chiitiko kugadzirisa chiitiko, kuvandudza pharmacokinetic properties, uye kubatsira kutsvagisa nekuvandudzwa kwemishonga mitsva, inotarisirwa kushandiswa pakurapa zvirwere zvakasiyana-siyana.
Organic synthesis: Sechivharo chakakosha chekuvaka, inotora chikamu mukuvaka kweiyo yakazara synthesis yezvakaoma zvigadzirwa zvechisikigo uye kugadzirira kwezvinhu zvitsva zve organic zvinoshanda, inosimudzira kusimukira kwemunda we organic chemistry, uye inopa hwaro hwekugadzirwa kwezvinhu zvitsva. zvinhu.