723614

4-(ジフェニルアミノ)フェニルボロン酸 ピナコール エステル

95%

• 別名: N-(4-(4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン-2-イル)フェニル-N-フェニルベンゼンアミン, ジフェニル-[4-(4,4,5,5-テトラメチル-[1,3,2]ジオキサボロラン-2-イル)-フェニル]-アミン
• 実験式（ヒル表記法）: C₂₄H₂₆BNO₂
• 分子量: 371.28
• MDL番号: MFCD13195770
• UNSPSCコード: 12352103
• PubChem Substance ID: 329764021
• NACRES: NA.23

特性

• 品質水準: 100
• アッセイ: 95%
• フォーム: powder
• mp: 93-98 °C
• SMILES記法: CC1(C)OB(OC1(C)C)c2ccc(cc2)N(c3ccccc3)c4ccccc4
• InChI: 1S/C24H26BNO2/c1-23(2)24(3,4)28-25(27-23)19-15-17-22(18-16-19)26(20-11-7-5-8-12-20)21-13-9-6-10-14-21/h5-18H,1-4H3
• InChI Key: VKSWIFGDKIEVFZ-UHFFFAOYSA-N

詳細

詳細

4-(Diphenylamino)phenylboronic acid pinacol ester is an aryl boronic acid ester that is majorly used in organic synthesis. It can be used in the transition metal-catalyzed Suzuki-Miyaura cross-coupling reaction due to its low toxicity and unique reactivity. It is an electron rich boronic acid ester that can also be used in protodeboronation.

アプリケーション

4-(Diphenylamino)phenylboronic acid pinacol ester may be used to synthesize 4-(2,2′ -bithiophen-5-yl)- 5-phenylpyrimidine for potential usage in the development of sensing devices for the detection of nitroaromatic explosives. It can also be used in the synthesis of oligothiophene (electron donating group) for the fabrication of dye sensitized solar cells (DSSCs).

安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable