您当前所在的位置:首页 > 产品中心 > 产品信息
4-硝基苯硼酸_分子结构_CAS_24067-17-2)
点击图片或这里关闭

4-硝基苯硼酸

产品号 673854 公司名称 Sigma Aldrich
CAS号 24067-17-2 公司网站 http://www.sigmaaldrich.com
分子式 C6H6BNO4 电 话 1-800-521-8956
分子量 166.92714 传 真
纯 度 ≥95.0% 电子邮件
保 存 Chembase数据库ID: 64737

产品价格信息

请登录

产品别名

标题
4-Nitrophenylboronic acid
IUPAC标准名
(4-nitrophenyl)boronic acid
IUPAC传统名
4-nitrophenylboronic acid
别名
p-nitro-benzeneboronic acid
4-Nitrobenzeneboronic acid
p-Nitrophenylboronic acid

产品登记号

MDL号 MFCD00161360
PubChem SID 24885181
CAS号 24067-17-2

产品性质

线性分子式 (O2N)C6H4(B(OH)2)
纯度 ≥95.0%
熔点 285-290 °C (dec.)
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H302
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
危险公开号 22
德国WGK号 3

产品详细信息

详细说明 (English)
Other Notes
May contain varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reagent used for
• Ligand-free palladium-catalyzed Suzuki-Miyaura cross-couplings1
• Ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines2
• Diels-Alder or C-H activation reactions3
• Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulations4
• N-arylation of phenylurea using copper acetylacetonate catalyst5
• Environmentally benign one-pot synthesis through a double arylation process6
• Copper-mediated cyanations7
• copper-catalyzed arylations8
• Regioselective glycosylations9
• Suzuki couplings followed by arylations10
• X-ray absorption on rhodium-grafted hydrotalcite catalyst for heterogeneous 1,4-addition reaction of organoboron reagents to electron deficient olefins11 Reagent used in Preparation of
• Combretastatin analogs as potential antitumor agents12
• Human immunodeficiency virus (HIV) protease inhibitors with antiviral activities against drug-resistant viruses13
详细说明 (简体中文)
Other Notes
可能含不定量的酸酐
包装
1, 5 g in glass bottle
Application
Reagent used for
• Ligand-free palladium-catalyzed Suzuki-Miyaura cross-couplings1
• Ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines2
• Diels-Alder or C-H activation reactions3
• Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulations4
• N-arylation of phenylurea using copper acetylacetonate catalyst5
• Environmentally benign one-pot synthesis through a double arylation process6
• Copper-mediated cyanations7
• copper-catalyzed arylations8
• Regioselective glycosylations9
• Suzuki couplings followed by arylations10
• X-ray absorption on rhodium-grafted hydrotalcite catalyst for heterogeneous 1,4-addition reaction of organoboron reagents to electron deficient olefins11 Reagent used in Preparation of
• Combretastatin analogs as potential antitumor agents12
• Human immunodeficiency virus (HIV) protease inhibitors with antiviral activities against drug-resistant viruses13

参考文献