Iodomethylboronic acid pinacol ester

Product Number: I13324; CAS Number: 70557-99-2

I13324 Technical Data Sheet and Reactions

$28.00$1,048.00

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Iodomethylboronic acid pinacol ester 2-(Iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane CAS: 70557-99-2 MDL: MFCD12405515

Molecular weight:    267.90    g/mol

Molecular Formula: C7H14BIO2

CAS Number:  70557-99-2

Storage:               Store at 2-8 Co, under dry conditions.

Synonyms:   70557-99-2, 2-(iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Iodomethylboronic acid, pinacol ester, 1,3,2-Dioxaborolane, 2-(iodomethyl)-4,4,5,5-tetramethyl-, Iodomethyl boronic acid pinacol ester, 2-Iodomethyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, Pinacol iodomethaneboronate, SCHEMBL3197440

Uses:     Synthesis building block, Organic Synthesis, Transition Metal Coupling

Iodomethylboronic acid pinacol ester, is a synthetic fine chemical useful in the synthesis of pharmaceuticals and fine organic chemicals.

 Pinacol Ester Derivative Coupling Reactions

 Palladium(0)-Catalyzed Cross-Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters, Ishiyama, Tatsuo, Murata, Miki, Miyaura, Norio, Journal of Organic Chemistry (1995), 60(23), 7508-10. DOI:10.1021/jo00128a024

  1. Cross Coupling Reactions of Chiral Secondary Organoboronic Esters With Retention of Configuration, Imao, Daisuke, Glasspoole, Ben W., Laberge, Veronique S., Crudden, Cathleen M., Journal of the American Chemical Society (2009), 131(14), 5024-5025. DOI:10.1021/ja8094075

 

  1. Palladium-Catalyzed Cross-Coupling Reaction of Bis(pinacolato)diboron with 1-Alkenyl Halides or Triflates: Convenient Synthesis of Unsymmetrical 1,3-Dienes via the Borylation-Coupling Sequence, Takagi, Jun, Takahashi, Kou, Ishiyama, Tatsuo, Miyaura, Norio, Journal of the American Chemical Society (2002), 124(27), 8001-8006. DOI:10.1021/ja0202255

 

  1. Functionalized olefin cross-coupling to construct carbon-carbon bonds, Lo, Julian C., Gui, Jinghan, Yabe, Yuki, Pan, Chung-Mao, Baran, Phil S., Nature (London, United Kingdom) (2014), 516(7531), 343-348. DOI:10.1038/nature14006.

 

  1. The Synthesis of Highly Substituted Isoxazoles by Electrophilic Cyclization: An Efficient Synthesis of Valdecoxib, Waldo, Jesse P., Larock, Richard C., Journal of Organic Chemistry (2007), 72(25), 9643-9647. DOI:10.1021/jo701942e.

 

  1. Arenes to anilines and aryl ethers by sequential iridium-catalyzed borylation and copper-catalyzed coupling, Tzschucke, C. Christoph, Murphy, Jaclyn M., Hartwig, John F., Organic Letters (2007), 9(5), 761-764. DOI:10.1021/ol062902w

 

  1. A synthesis of allyboronates via the palladium(0)-catalyzed cross-coupling reaction of bis(pinacolato)diboron with allylic acetates, Ishiyama, Tatsuo, Ahiko, Taka-aki, Miyaura, Norio, Tetrahedron Letters (1996), 37(38), 6889-6892. DOI:10.1016/0040-4039(96)01505-5

 

  1. Rapid synthesis of 3-amino-imidazopyridines by a microwave-assisted four-component coupling in one pot, DiMauro, Erin F., Kennedy, Joseph M., Journal of Organic Chemistry (2007), 72(3), 1013-1016, DOI:10.1021/jo0622072

 

  1. 9. Iron-Catalyzed C(sp2)-H Bond Functionalization with Organoboron Compounds, Shang, Rui, Ilies, Laurean, Asako, Sobi, Nakamura, Eiichi, Journal of the American Chemical Society (2014), 136(41), 14349-14352. DOI:10.1021/ja5070763

 

  1. Copper-Promoted Coupling of Vinyl Boronates and Alcohols: A Mild Synthesis of Allyl Vinyl Ethers, Shade, Ryan E., Hyde, Alan M., Olsen, John-Carl, Merlic, Craig A., Journal of the American Chemical Society (2010), 132(4), 1202-1203. DOI:10.1021/ja907982w
Categories

Purity %

0.98

Molecular Formula

C7H14BIO2

Molecular Weight

267.9

CAS #

70557-99-2

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