ʻO Isopropenylboronic Acid Pinacol Ester CAS 126726-62-3 Maʻemaʻe> 99.0% (GC) Hale Hana Kiʻekiʻe
Mea Manufacturer lako me High Quality, Commercial Production
Inoa Kemika: Isopropenylboronic Acid Pinacol Ester
CAS: 126726-62-3
Inoa Kimia | ʻO Isopropenylboronic Acid Pinacol Ester |
Nā huaʻōlelo like | 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl) -1,3,2-dioxaborolane;2-(1-Methylethenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
Helu CAS | 126726-62-3 |
Helu CAT | RF-PI1395 |
Kūlana Kūʻai | Ma ka waihona, ʻoi aku ka nui o ka hana a hiki i nā tona |
ʻĀpana Molekala | C9H17BO2 |
Kaumaha Molecular | 168.04 |
Brand | Kemika Ruifu |
'ikamu | Nā kikoʻī |
Ka nana aku | ʻAʻole waihoʻoluʻu i ka wai melemele ʻeleʻele |
Maʻemaʻe / Kaʻina Hanana | >99.0% (GC) |
Māmā (KF) | ≤0.50% |
Huina paumaele | <1.00% |
Kūlana hoʻāʻo | ʻOihana Kūlana |
Hoʻohana | Nā Kūwaena Lapaʻau |
Pūʻolo: ʻO ka'ōmole, 25kg / Barrel, aiʻole e like me ka makemake o ka mea kūʻai.
Kūlana mālama:E mālama i loko o nā pahu i hoʻopaʻa ʻia ma kahi maloʻo a maloʻo;E pale i ka malamalama a me ka wai.
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ʻO ka Isopropenylboronic Acid Pinacol Ester (CAS: 126726-62-3) he mea hoʻohui ester maʻamau i hoʻohana ʻia no ka palladium-catalyzed Suzuki-Miyaura cross-coupling process, inverse-electron-demand Diels-Alder reaction, Simmons-Smith cyclopropanation reaction, polyene cyclization stereoselective aldol reactions, Grubbs cross-metathesis reaction, intramolecular Suzuki-Miyaura reaction, Stereoselective cross-metathesis, dipolar cycloaddition, iodosulfonylation, asymmetric conjugate hoʻohui a me intramolecular hydroacylation a me ka hoʻomākaukau ʻana i nā ʻano therapeutic kinase a me nā mea hoʻopaneʻe enzymatic.Hiki ke hoʻohana ʻia ʻo Isopropenylboronic Acid Pinacol Ester ma ke ʻano he waena i ka synthesis o nā ʻano mea like ʻole a me ka acyclic organik.Ua hōʻike ʻia hoʻi e hiki ke hoʻohana ʻia ka α-Substituted Allyl/Croty o kēia pūhui no ka Diastereoand Enantioselective allylboration o nā aldehydes kiʻekiʻe.