4-甲酰基苯硼酸

• 产品号: 431966
• CAS号: 87199-17-5
• 分子式: C7H7BO3
• 分子量: 149.93968
• 纯 度: ≥95.0%

产品别名

• 标题: 4-Formylphenylboronic acid
• IUPAC标准名: (4-formylphenyl)boronic acid
• IUPAC传统名: 4-formylphenylboronic acid
• 别名: 4-Boronobenzaldehyde; 4-(Dihydroxyboryl)benzaldehyde; 对甲酰苯硼酸; 4-Formylbenzeneboronic acid; p-Formylbenzeneboronic acid; p-Formylphenylboronic acid; 4-醛基苯硼酸

产品登记号

• PubChem SID: 24867058
• Beilstein号: 3030770
• CAS号: 87199-17-5
• MDL号: MFCD00151823

产品性质

• GHS警示词: Danger
• GHS危险声明: H314-H317
• 欧盟危险性物质标志: 腐蚀性(Corrosive) (C)
• 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
• GHS警示性声明: P280-P305 + P351 + P338-P310
• RID/ADR: UN 1759 8/PG 3
• 危险公开号: 34
• 安全公开号: 22-26-36/37/39-45
• 联合国危险货物等级: 8
• 联合国危险货物编号: 1759
• 联合国危险货物包装类别(PG): 3
• 德国WGK号: 3
• 线性分子式: HCOC6H4B(OH)2
• 纯度: ≥95.0%
• 熔点: 237-242 °C(lit.)

产品详细信息

详细说明 (简体中文)

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

详细说明 (English)

Other Notes
Contains varying amounts of anhydride
Packaging
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