反丙烯硼酸

• 产品号: 576638
• CAS号: 7547-97-9
• 分子式: C3H7BO2
• 分子量: 85.89748
• 纯 度: ≥95.0%

产品别名

• 标题: trans-1-Propen-1-ylboronic acid
• IUPAC标准名: [(1E)-prop-1-en-1-yl]boronic acid
• IUPAC传统名: (1E)-prop-1-en-1-ylboronic acid
• 别名: trans-1-Propenylboronic acid; (E)-Prop-1-enylboronic acid; (E)-1-Propen-1-ylboronic acid; trans-1-Propeneboronic acid; trans-Propenylboronic acid

产品登记号

• PubChem SID: 24880870
• MDL号: MFCD02179501
• CAS号: 7547-97-9

产品性质

• 杂质: ~10 wt. % cis-isomer
• 线性分子式: CH3CH=CHB(OH)2
• 纯度: ≥95.0%
• 熔点: 123-127 °C(lit.)
• 个人保护装置: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• 保存温度: 2-8°C
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3Reactant for preparation of:
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization6
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones7
Reactant for
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3
• Palladium-catalyzed Sonogashira cross-coupling7 Reactant for preparation of
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones

详细说明 (简体中文)

Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Other Notes
含有不定量的酸酐
包装
1, 5 g in glass bottle
Application
Reactant for:
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3Reactant for preparation of:
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization6
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones7
Reactant for
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3
• Palladium-catalyzed Sonogashira cross-coupling7 Reactant for preparation of
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones