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(2-甲酰基-4,5-亚甲二氧基)苯基硼酸_分子结构_CAS_94838-88-7)
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(2-甲酰基-4,5-亚甲二氧基)苯基硼酸

产品号 717622 公司名称 Sigma Aldrich
CAS号 94838-88-7 公司网站 http://www.sigmaaldrich.com
分子式 C8H7BO5 电 话 1-800-521-8956
分子量 193.94918 传 真
纯 度 ≥95% 电子邮件
保 存 Chembase数据库ID: 74771

产品价格信息

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产品别名

标题
2-Formyl-4,5-methylenedioxyphenylboronic acid
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

产品登记号

CAS号 94838-88-7
MDL号 MFCD01319005

产品性质

Empirical Formula (Hill Notation) C8H7BO5
纯度 ≥95%
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26-36
德国WGK号 2

产品详细信息

详细说明 (English)
Packaging
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
详细说明 (简体中文)
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

参考文献