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吡啶-3-硼酸

吡啶-3-硼酸用途

吡啶-3-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。

吡啶-3-硼酸名称

[ CAS 号 ]:
1692-25-7

[ 中文名 ]:
吡啶-3-硼酸

[ 英文名 ]:
3-Pyridylboronic acid

[中文别名 ]:

3-吡啶硼酸

[英文别名 ]:

Acide pyridin-3-ylboronique
3-Pyridineboronic acid
Pyridin-3-bronic Acid
3-Pridylboronic acid
pyridin-3-yl boronic acid
3-Pyridylboronic aci
3-Pyridinylboronic acid
Boronic acid, B-3-pyridinyl-
pyridin-3-ylboronic acid
RARECHEM AH PB 0251

吡啶-3-硼酸生物活性

[ 描述 ]:

吡啶-3-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

吡啶-3-硼酸物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
308.8±34.0 °C at 760 mmHg

[ 熔点 ]:
>300 °C(lit.)

[ 分子式 ]:
C₅H₆BNO₂

[ 分子量 ]:
122.92

[ 闪点 ]:
140.5±25.7 °C

[ 精确质量 ]:
123.049156

[ PSA ]:
53.35000

[ LogP ]:
0.10

[ 外观性状 ]:
淡黄色粉末

[ 蒸汽压 ]:
0.0±0.7 mmHg at 25°C

[ 折射率 ]:
1.534

[ 储存条件 ]:
0-6°C

[ 水溶解性 ]:
水溶性：不溶

吡啶-3-硼酸MSDS

吡啶-3-硼酸安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ 危害码 (欧洲) ]:
Xn:Harmful

[ 风险声明 (欧洲) ]:
R22;R36/37/38

[ 安全声明 (欧洲) ]:
S36/37/39-S3-S26

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

[ WGK德国 ]:
3

[ 海关编码 ]:
2933399090

吡啶-3-硼酸合成路线

吡啶-3-硼酸上下游产品

吡啶-3-硼酸上游产品

吡啶-3-硼酸下游产品

吡啶-3-硼酸海关

[ 海关编码 ]: 2933399090

[ 中文概述 ]:
2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

吡啶-3-硼酸文献

A new access to 3-substituted-1(2H)-isoquinolone by tandem palladium-catalyzed intramolecular aminocarbonylation annulation.

Org. Biomol. Chem. 13th ed., 10 , 2683-2691, (2012)

An original tribromide derivative based, palladium-catalyzed synthesis of 3-substituted-1(2H)-isoquinolone is described based on a regioselective Suzuki-Miyaura C-C coupling on o-halo-(2,2-dihalovinyl...

Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors.

Bioorg. Med. Chem. Lett. 5th ed., 22 , 1976-1979, (2012)

A series of P1-substituted biaryl amprenavir derivatives was designed and synthesized. These compounds were evaluated for enzyme inhibition and antiviral activity in vitro. Several compounds showed hi...

Copper-mediated sequential cyanation of aryl C-B and arene C-H bonds using ammonium iodide and DMF.

J. Am. Chem. Soc. 5th ed., 134 , 2528-2531, (2012)

The cyanation of aromatic boronic acids, boronate esters, and borate salts was developed under copper-mediated oxidative conditions using ammonium iodide and DMF as the source of nitrogen and carbon a...

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