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Merck

522554

Sigma-Aldrich

2-羟基苯硼酸频哪醇酯

98%

别名:

2-(4,4,5,5-四甲基-1,3,2-二杂氧戊硼烷-2-基)苯酚

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About This Item

经验公式(希尔记法):
C12H17BO3
分子量:
220.07
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

化驗

98%

折射率

n20/D 1.506 (lit.)

bp

282 °C (lit.)

密度

1.05 g/mL at 25 °C (lit.)

SMILES 字串

CC1(C)OB(OC1(C)C)c2ccccc2O

InChI

1S/C12H17BO3/c1-11(2)12(3,4)16-13(15-11)9-7-5-6-8-10(9)14/h5-8,14H,1-4H3

InChI 密鑰

VLROJECCXBBKPZ-UHFFFAOYSA-N

應用

Reactant involved in:
  • Synthesis of indolo-fused heterocyclic inhibitors of polymerase enzyme of hepatitis C
  • Studies of pi-interactions, electronic structure and transient UV absorption of subphthalocyanine-borate-bridged ferrocene-fullerene conjugates
  • Synthesis of subphthalocyanine and fused-ring nicotine derivatives
  • Suzuki-Miyaura coupling-triflation sequence, reduction and salt formation for synthesis of hydroxylated oligoarene phosphines
广泛用于 Suzuki 偶联反应。

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析证书(COA)

Lot/Batch Number

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其他客户在看

Tetrahedron, 58, 9633-9695 (2002)

商品

The synthesis of biaryl compounds via the Suzuki coupling reaction has become more commonplace now that many arylboronic acids are readily available. We are pleased to offer arylboronic acid pinacol esters4 as part of a growing line of products used in the Suzuki coupling reaction.

The synthesis of biaryl compounds via the Suzuki coupling reaction has become more commonplace now that many arylboronic acids are readily available. We are pleased to offer arylboronic acid pinacol esters4 as part of a growing line of products used in the Suzuki coupling reaction.

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