I-1-Phenylvinylboronic Acid CAS 14900-39-1 Purity >98.0% (GC) Factory High Quality

Incazelo emfushane:

Igama Lekhemikhali: 1-Phenylvinylboronic Acid

I-CAS: 14900-39-1

Ubumsulwa: >98.0% (GC)

Ukubukeka: Okumhlophe Okumhlophe ukuya Kokuphuzi Okuqinile Okukhanyayo

Ikhwalithi Ephezulu, Ukukhiqizwa Kwezohwebo

E-Mail: alvin@ruifuchem.com


Imininingwane Yomkhiqizo

Imikhiqizo Ehlobene

Omaka bomkhiqizo

Incazelo:

Ukuhlinzeka Ngomkhiqizi Ngekhwalithi Ephezulu, Ukukhiqiza Kwezentengiso
Igama Lekhemikhali: 1-Phenylvinylboronic Acid CAS: 14900-39-1

Chemical Properties:

Igama Lekhemikhali I-1-Phenylvinylboronic Acid
Omqondofana i-α-Phenylvinylboronic Acid;(1-Phenylethenyl)i-boronic Acid
Inombolo ye-CAS 14900-39-1
Inombolo yeCAT I-RF-PI1435
Isimo Sesitoko Esitokweni, Isikali Sokukhiqiza Sifinyelela Kumathani
I-Molecular Formula C8H9BO2
Isisindo samangqamuzana 147.97
I-Melting Point 125℃ (dec.) (lit.)
Ibhrendi I-Ruifu Chemical

Imininingwane:

Into Imininingwane
Ukubukeka Okuqinile Okumhlophe kuya Kokuphuzi Okukhanyayo
Ukuhlanzeka / Indlela Yokuhlaziya >98.0% (GC)
Ukulahlekelwa Ekumisweni ≤1.00%
Ukungcola Okuphelele <2.00%
I-Infrared Spectrum Ivumelana Nesakhiwo
I-NMR Ivumelana Nesakhiwo
Izinga Lokuhlola I-Enterprise Standard
Ukusetshenziswa Pharmaceutical Intermediates

Iphakheji nesitoreji:

Iphakheji: Ibhodlela, isikhwama se-Aluminium foil, 25kg/Cardboard Drum, noma ngokwezidingo zekhasimende.

Isimo Sesitoreji:Gcina ezitsheni ezivaliwe endaweni epholile neyomile;Vikela ekukhanyeni nakumswakama.

Izinzuzo:

1

I-FAQ:

Isicelo:

I-1-Phenylvinylboronic Acid (i-CAS: 14900-39-1) I-Reactant ehilelekile ku: I-Halogenation ye-alkynes yokulungiswa kwe-enol esters;Ukuhlanganisa i-Liebeskind-Srogl;I-Homocoupling ye-arylboronic acid yokuhlanganiswa kwe-biaryls;Ukuhlanganisa okuphindaphindiwe kwamabhulokhi wokwakha we-boronate;I-hydrogenation enantioselective ye-hydroxyphenyl styrenes;I-Samarium diiodide-mediated cyclization yokuhlanganiswa kwe-benzannulated cyclooctanol derivatives esikhundleni;I-Suzuki-Miyaura cross-coupling for synthesis of C-6-substituted uridine phosphonates.

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