物质信息
ID:316099
名称和标识
IUPAC传统名
4-formylphenylboronic acid
IUPAC标准名
(4-formylphenyl)boronic acid
别名
4-Boronobenzaldehydep-Formylphenylboronic acid4-(Dihydroxyboryl)benzaldehyde4-醛基苯硼酸对甲酰苯硼酸4-Formylbenzeneboronic acid4-Formylphenylboronic acid4-甲酰基苯硼酸p-Formylbenzeneboronic acid
化合物性质
安全信息
GHS危险品标识
腐蚀金属，类别1
腐蚀皮肤，类别1A，1B，1C
严重眼损伤，类别1
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
安全公开号
22-26-36/37/39-45
联合国危险货物包装类别(PG)
3
个人保护装置
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
危险公开号
34
联合国危险货物等级
8
GHS危险声明
H314-H317
MSDS下载
联合国危险货物编号
1759
德国WGK号
3
欧盟危险性物质标志
腐蚀性 (C)GHS警示性声明
P280-P305+P351+P338-P310
RID/ADR
UN 1759 8/PG 3
GHS警示词
Danger
产品相关信息
纯度
≥95.0%
线性分子式
HCOC6H4B(OH)2
理化性质
熔点
237-242 °C(lit.)
描述信息
Other Notes
含不定量的酸酐
包装
1, 5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water1
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2
• Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids3
• Triethylamine-catalyzed three-component Hantzsch condensations4
• Copper-catalyzed nitrations5
• Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta6
• Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides7
• Palladium-catalyzed aerobic oxidative cross-coupling reactions8 Reagent used in Preparation of
• Sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells9
• A novel protein synthesis inhibitor active against Gram-positive bacteria10
含不定量的酸酐
包装
1, 5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water1
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2
• Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids3
• Triethylamine-catalyzed three-component Hantzsch condensations4
• Copper-catalyzed nitrations5
• Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta6
• Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides7
• Palladium-catalyzed aerobic oxidative cross-coupling reactions8 Reagent used in Preparation of
• Sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells9
• A novel protein synthesis inhibitor active against Gram-positive bacteria10
分子图谱
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参考文献
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