物质信息
ID:321627
名称和标识
IUPAC标准名
(6-formyl-2H-1,3-benzodioxol-5-yl)boronic acid
IUPAC传统名
6-formyl-2H-1,3-benzodioxol-5-ylboronic acid
别名
2-Formyl-4,5-methylenedioxyphenylboronic acid(2-甲酰基-4,5-亚甲二氧基)苯基硼酸
化合物性质
安全信息
危险公开号
36/37/38
德国WGK号
2
安全公开号
26-36
GHS危险声明
H315-H319-H335
欧盟危险性物质标志
刺激性 (Xi)GHS危险品标识
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
GHS警示词
Warning
MSDS下载
GHS警示性声明
P261-P305+P351+P338
产品相关信息
Empirical Formula (Hill Notation)
C8H7BO5
纯度
≥95%
描述信息
包装
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective preparation of indenamines by cationic palladium complex-catalyzed tandem annulation with alkynes1
• Stereoselective preparation of indenol derivatives via cationic palladium complex-catalyzed diastereoselective tandem annulation2
• Synthesis of oxazoline-substituted potassium organotrifluoroborates3
• Preparation of aristolactam analogs as an antitumor agent4
• Suzuki-Miyaura coupling reactions5
• Suzuki and Negishi cross-coupling reactions6
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective preparation of indenamines by cationic palladium complex-catalyzed tandem annulation with alkynes1
• Stereoselective preparation of indenol derivatives via cationic palladium complex-catalyzed diastereoselective tandem annulation2
• Synthesis of oxazoline-substituted potassium organotrifluoroborates3
• Preparation of aristolactam analogs as an antitumor agent4
• Suzuki-Miyaura coupling reactions5
• Suzuki and Negishi cross-coupling reactions6
分子图谱
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参考文献
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