物质信息

ID:316793

名称和标识
IUPAC标准名
(4-nitrophenyl)boronic acid
IUPAC传统名
4-nitrophenylboronic acid
别名
p-nitro-benzeneboronic acid4-硝基苯硼酸4-Nitrobenzeneboronic acidp-Nitrophenylboronic acid4-Nitrophenylboronic acid
数据登录号
PubChem SID
化合物性质
安全信息
MSDS下载
德国WGK号
3
欧盟危险性物质标志
有害性 有害性 (Xn)
危险公开号
22
GHS警示词
Warning
GHS危险品标识
GHS07
急性毒性(口服,皮肤接触,吸入),类别4
皮肤刺激,类别2
眼刺激,类别2
皮肤过敏,类别1
特定目标器官毒性 -一次接触,类别3
个人保护装置
dust mask type N95 (US), Eyeshields, Gloves
GHS危险声明
H302
产品相关信息
纯度
≥95.0%
线性分子式
(O2N)C6H4(B(OH)2)
理化性质
熔点
285-290 °C (dec.)
描述信息
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
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参考文献
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