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Merck
CN
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文件

346225

Sigma-Aldrich

(2-甲基丙基)硼酸

≥95.0%

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别名:
异丁基硼酸
线性分子式:
(CH3)2CHCH2B(OH)2
CAS号:
84110-40-7
分子量:
101.94
MDL编号:
MFCD00134156
UNSPSC代码:
12352103
PubChem化学物质编号:
24861382
NACRES:
NA.22

质量水平

200

检测方案

≥95.0%

形式

solid

mp

108-111 °C (lit.)

SMILES字符串

CC(C)CB(O)O

InChI

1S/C4H11BO2/c1-4(2)3-5(6)7/h4,6-7H,3H2,1-2H3

InChI key

ZAZPDOYUCVFPOI-UHFFFAOYSA-N

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应用

（2-甲基丙基）硼酸可用作：    
  • 通过与4-溴异喹啉的Suzuki-Miyaura偶联反应制备4-异丁基异喹啉的反应物。
  • 与氢氧化铝和硼酸一起用作苯乙烯聚合的催化剂。

它还可用作以下反应的反应物：    
  • 铜催化的交叉偶联反应。      
  • 通过铱催化的C-H硼化反应合成聚硼基烷。        
  • 杂取代二氮杂硼杂环戊二烯和硼杂环化合物的制备。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

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Study of Rate-accelerating of Aluminum Hydroxide, Boric Acid, and (2-Methylpropyl) Boronic Acid for Atom Transfer Radical Polymerization of Styrene
Luo Yu-tai, et al.
Journal of Xiamen University (Natural Science), 47(1), 63-63 (2008)
Steven A Rossi et al.
Organic letters, 15(9), 2314-2317 (2013-04-25)
For the first time, a general catalytic procedure for the cross-coupling of primary amides and alkylboronic acids is demonstrated. The key to the success of this reaction was the identification of a mild base (NaOSiMe3) and oxidant (di-tert-butyl peroxide) to
Solution-state 15N NMR and solid-state single-crystal XRD study of heterosubstituted diazaboroles and borinines prepared via an effective and simple microwave-assisted solvent-free synthesis
Slabber CA, et al.
Journal of Organometallic Chemistry, 723, 122-128 (2013)
Takeshi Yamamoto et al.
Organic letters, 21(16), 6235-6240 (2019-08-07)
Pyrazolylaniline serves as a temporary directing group attached to the boron atom of alkylboronic acids in Ir-catalyzed C(sp3)-H borylation. The reaction takes place at α-, β-, and γ-C-H bonds, giving polyborylated products including di-, tri-, tetra-, and even pentaborylalkanes. α-C-H
Benjamin M Reeves et al.
Angewandte Chemie (International ed. in English), 58(44), 15697-15701 (2019-09-06)
A transition-metal-free reductive hydroxymethylation reaction has been developed, enabling the preparation of tetrahydroisoquinolines bearing C4-quaternary centers from the corresponding isoquinolines. Deuterium labelling studies and control experiments enable a potential mechanism to be elucidated which features a key Cannizzaro-type reduction followed
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