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4-(三氟甲基)苯硼酸

4-(三氟甲基)苯硼酸用途

4-三氟甲基苯基硼酸是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

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4-(三氟甲基)苯硼酸名称

[ CAS 号 ]:
128796-39-4

[ 中文名 ]:
4-三氟甲基苯硼酸

[ 英文名 ]:
4-Trifluoromethylphenylboronic acid

[中文别名 ]:

[英文别名 ]:

QBQR DXFFF
MFCD00151855
4-(Trifluoromethyl)phenylboronic acid
Boronic acid, B-[4-(trifluoromethyl)phenyl]-
α,α,α-Trifluoro-p-tolueneboronic Acid
Dihydroxy[4-(trifluoromethyl)phenyl]borane
α,α,α-Trifluoro-p-tolylboronic acid
(4-(Trifluoromethyl)phenyl)boronic acid
4-(Trifluoromethyl)benzeneboronic acid
[4-(Trifluoromethyl)phenyl]boranediol

4-(三氟甲基)苯硼酸生物活性

[ 描述 ]:

4-三氟甲基苯基硼酸是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

信号通路 >> 其他 >> 其他

[体外研究]

4-三氟甲基苯基硼酸用于通过铜交换的氟磷灰石对咪唑和胺进行 N个-芳基化,以及用于微波促进的与酰氯的交叉偶联,从而生成芳基酮。

4-(三氟甲基)苯硼酸物理化学性质

[ 密度 ]:
1.4±0.1 g/cm3

[ 沸点 ]:
258.6±50.0 °C at 760 mmHg

[ 熔点 ]:
245-250 °C(lit.)

[ 分子式 ]:
C₇H₆BF₃O₂

[ 分子量 ]:
189.93

[ 闪点 ]:
110.2±30.1 °C

[ 精确质量 ]:
190.041290

[ PSA ]:
40.46000

[ LogP ]:
2.16

[ 外观性状 ]:
白色粉末

[ 蒸汽压 ]:
0.0±0.6 mmHg at 25°C

[ 折射率 ]:
1.462

[ 储存条件 ]:
0-6°C

[ 水溶解性 ]:
可溶于：甲醇

4-(三氟甲基)苯硼酸MSDS

4-(三氟甲基)苯硼酸安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H302

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi:Irritant

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S37/39-S26

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
2931900090

4-(三氟甲基)苯硼酸合成路线

4-(三氟甲基)苯硼酸上下游产品

4-(三氟甲基)苯硼酸上游产品

4-(三氟甲基)苯硼酸下游产品

4-(三氟甲基)苯硼酸海关

[ 海关编码 ]: 2931900090

[ 中文概述 ]:
2931900090. 其他有机-无机化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:AB(入境货物通关单,出境货物通关单). 最惠国关税:6.5%. 普通关税:30.0%

[ Summary ]:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

4-(三氟甲基)苯硼酸文献

Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.

Org. Lett. 7th ed., 14 , 1930-1933, (2012)

A Ru-catalyzed direct arylation of benzylic sp(3) carbons of acyclic amines with arylboronates is reported. This highly regioselective and efficient transformation can be performed with various combin...

Tandem-type Pd(II)-catalyzed oxidative Heck reaction/intramolecular C-H amidation sequence: a novel route to 4-aryl-2-quinolinones.

Chem. Commun. (Camb.) 36th ed., 48 , 4332-4334, (2012)

A novel catalytic method for synthesizing 4-aryl-2-quinolinones is reported. The process involves two mechanistically independent, sequential Pd(II)-catalyzed reactions--the oxidative Heck reaction an...

Combined experimental-theoretical NMR study on 2,5-bis(5-aryl-3-hexylthiophen-2-yl)-thiazolo[5,4-d]thiazole derivatives for printable electronics.

Magn. Reson. Chem. 5th ed., 50 , 379-387, (2012)

Four 2,5-bis(5-aryl-3-hexylthiophen-2-yl)thiazolo[5,4-d]thiazole derivatives have been synthesized and thoroughly characterized. The extended aromatic core of the molecules was designed to enhance the...

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