| 产品名称 | 4-乙酰苯硼酸 (含不同量的酸酐) |
|---|---|
| 英文名称 | 4-Acetylbenzeneboronic Acid (contains varying amounts of Anhydride) |
| 别名 | 对醛基苯硼酸;对醛基苯硼酸(含不同量的酸酐) |
| 英文别名 | 4-Acetylbenzeneboronic Acid 4'-Boronoacetophenone;4-Acetylphenylboronic Acid (contains varying amounts of Anhydride) |
| 应用 | 4-Acetylphenylboronic acid was used in the synthesis of 4′-azidoacetophenone. Reactant involved in: · Palladium-catalyzed decarboxylative coupling · Copper-catalyzed hydroxylation · Palladium-catalyzed Suzuki-Miyaura cross-coupling · Cross-coupling with α-bromocarbonyl compounds · Oxidation catalyzed by Baeyer-Villiger monooxygenases · 1,5-substitution reactions |
| 规格或纯度 | 98% |
| 运输条件 | 常规运输 |
4-Acetylphenylboronic acid is a boronate, belongs to a class of synthetic organic compounds. It reacts rapidly with peroxynitrite (ONOO(-)) to form stable hydroxy derivatives.It undergoes Suzuki coupling with 4-bromotriphenylamine catalyzed by dichlorobis(triphenylphosphine)Pd(II), during the synthesis of dendrimers4-Acetylphenylboronic acid was used in the synthesis of 4′-azidoacetophenone. Reactant involved in: · Palladium-catalyzed decarboxylative coupling · Copper-catalyzed hydroxylation · Palladium-catalyzed Suzuki-Miyaura cross-coupling · Cross-coupling with α-bromocarbonyl compounds · Oxidation catalyzed by Baeyer-Villiger monooxygenases · 1,5-substitution reactions
4-Acetylphenylboronic acid is a boronate, belongs to a class of synthetic organic compounds. It reacts rapidly with peroxynitrite (ONOO(-)) to form stable hydroxy derivatives.It undergoes Suzuki coupling with 4-bromotriphenylamine catalyzed by dichlorobis(triphenylphosphine)Pd(II), during the synthesis of dendrimers
| 标识符号 | GHS07 |
|---|---|
| 警示性声明 | P261,P305+P351+P338 |
| 危害声明 | H315,H319,H335 |
| 个人防护设备 | dust mask type N95 (US),Eyeshields,Gloves |
| WGK | 3 |
| CAS编号 | 149104-90-5 |
|---|---|
| 敏感性 | 对湿度敏感 |
| 熔点 | 243-247°C |
| 溶解性 | 不溶于水;可溶于甲醇 |
| 储存温度 | 充氩 |
| Reaxys-RN | 7869162 |
| MDL号 | MFCD01074667 |
| 密度 | 1.19 |
| 分子量 | 163.97 |
| 分子式 | C8H9BO3 |
| 品牌 | 阿拉丁 |
| PubChem CID | 3702122 |