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4-甲氧羰基苯硼酸_分子结构_CAS_99768-12-4)
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4-甲氧羰基苯硼酸

产品号 594539 公司名称 Sigma Aldrich
CAS号 99768-12-4 公司网站 http://www.sigmaaldrich.com
分子式 C8H9BO4 电 话 1-800-521-8956
分子量 179.96566 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 10043

产品价格信息

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产品别名

标题
4-Methoxycarbonylphenylboronic acid
IUPAC标准名
[4-(methoxycarbonyl)phenyl]boronic acid
IUPAC传统名
4-(methoxycarbonyl)phenylboronic acid
别名
(4-Carbomethoxyphenyl)boronic acid
p-(Methoxycarbonyl)boronic acid
4-甲酸甲酯苯硼酸
Methyl 4-boronobenzoate
4-Carbomethoxybenzeneboronic acid
4-Methoxycarbonylbenzeneboronic acid
4-borono-benzoic acid 1-methyl ester
p-(Methoxycarbonyl)phenylboronic acid
p-borono-benzoic acid methyl ester
Methyl p-boronobenzoate

产品登记号

MDL号 MFCD01632203
PubChem SID 24881520
CAS号 99768-12-4

产品性质

Empirical Formula (Hill Notation) C8H9BO4
熔点 197-200 °C(lit.)
MSDS下载 下载链接
个人保护装置 Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
德国WGK号 3

产品详细信息

详细说明 (English)
Other Notes
Contains varying amount of anhydride
Packaging
1, 5 g in glass bottle
Application
Reagent used for
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence1
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2
• One-pot ipso-nitration of arylboronic acids3
• Copper-catalyzed nitration4
• Cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling5
• Reagent used in Preparation of
• Biaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid6†
• Chromenones and their bradykinin B1 antagonistic activit7†
• Pt nanoparticles@Photoactive metal-organic frameworks resulting in efficient hydrogen evolution via synergistic photoexcitation and electron injectio8†
• Salicylate-based thienylbenzoic acids as E. coli methionine aminopeptidase inhibitor9†
详细说明 (简体中文)
Other Notes
含不定量的酸酐
包装
1, 5 g in glass bottle
Application
Reagent used for
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence1
• Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides2
• One-pot ipso-nitration of arylboronic acids3
• Copper-catalyzed nitration4
• Cyclocondensation followed by palladium-phosphine-catalyzed Suzuki-Miyaura coupling5
• Reagent used in Preparation of
• Biaryls via nickel-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl halides with arylboronic acid6†
• Chromenones and their bradykinin B1 antagonistic activit7†
• Pt nanoparticles@Photoactive metal-organic frameworks resulting in efficient hydrogen evolution via synergistic photoexcitation and electron injectio8†
• Salicylate-based thienylbenzoic acids as E. coli methionine aminopeptidase inhibitor9†

参考文献