物质信息

ID:336238

名称和标识
IUPAC标准名
4-(dihydroxyboranyl)benzoic acid
IUPAC传统名
4-carboxyphenylboronic acid
别名
4-(Dihydroxyboronyl)benzoic acid4-Boronobenzoic acid4-(Dihydroxyboryl)benzoic acidNSC 2211704-硼酸苯甲酸p-Boronobenzoic acidp-Carboxybenzeneboronic acidp-Carboxyphenylboronic acid4-羧基苯基硼酸4-Carboxyphenylboronic acid4-羧基苯硼酸4-Hydroxycarbonylphenyl boronic acid4-Carboxybenzeneboronic acid4-Carboxylphenylboronic acid
数据登录号
Beilstein号
PubChem SID
化合物性质
理化性质
熔点
220 °C (dec.)(lit.)
安全信息
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
MSDS下载
德国WGK号
2
RTECS编号
CY8925000
产品相关信息
线性分子式
HO2CC6H4B(OH)2
描述信息
包装
1, 10 g in glass bottle
Application
Reactant involved in:
• Condensation reactions with stabilizer chains at the surface of polystyrene latex1
• Suzuki coupling reactions2
• Esterification3
• Derivatization of polyvinylamine4
• Synthesis of isotopically labeled mercury5
• Functionalization of poly-SiNW for detection of dopamine6
Reagent used for
• Suzuki-Miyaura cross-coupling
• Induction of pH sensitivity on fluorescence lifetime of quantum dots by NIR fluorescent dyes
• Bio-supported palladium nanoparticles as phosphine-free catalyst for Suzuki reaction in water
• Chan-Lam-type Copper (Cu)-catalyzed S-arylation with aryl boronic acids at room temperatureReagent used in Preparation of
• Isoquinolones via regioselective Suzuki-Miyaura cross-coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation
• Amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors
• Phenols via visible-light initiated aerobic oxidative hydroxylation of arylboronic acids using air as oxidant catalyzed by Ruthenium (Ru)-complex
• Glucose sensitive boronic acid-bearing block copolymers
• Trisulfonated calixarene upper-rim sulfonamido derivatives and their complexation with the trimethyllysine epigenetic mark
分子图谱
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参考文献
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