4-(Hydroxymethyl)benzeneboronic acid 4-羟甲基苯硼酸
CAS 59016-93-2 MFCD00792672
化学结构图
SMILES: OCC1=CC=C(C=C1)B(O)O
化学属性
| Mol. Formula | C7H9BO3 |
|---|---|
| Mol. Weight | 152 |
| Melting Point | 287-289 |
| TSCA | No |
| Density | 1.25 |
别名和识别编码
| Chemical Name | 4-(Hydroxymethyl)benzeneboronic acid |
|---|---|
| CAS Number | 59016-93-2 |
| Alfabeta Name | HYDROXYMETHYLPHENYLBORONICACID 4()- |
| MDL Number | MFCD00792672 |
| Synonym | α-Hydroxy-p-tolueneboronic acid 4-Hydroxymethylbenzeneboronic acid 4-(Hydroxymethyl)phenylboronic acid α-Hydroxy-p-tolueneboronic acid 4-羟甲基苯硼酸 4-Hydroxymethylbenzeneboronic acid α-Hydroxy-p-tolueneboronic acid |
| PubChem Substance ID | 87559798 |
| Reaxys-RN | 2831413 |
| EC Number | 000-000-0 |
| Beilstein Registry Number | 2831413 |
| Chemical Name Translation | 4-羟甲基苯硼酸 |
| LabNetwork Molecule ID | LN00221562 |
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信息真实价格透明
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分类
- {SNA} Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids, Organometallic Reagents
- Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids, Organometallic Reagents
相关文献及参考
- 1. D. S. Mortensen, et al., , Discovery and SAR exploration of a novel series of imidazo[4,5-b]pyrazin-2-ones as potent and selective mTOR kinase inhibitors Bioorg. Med. Chem. Lett. 21 , 6793-6799, (2011)
- 2. F. Ye, et al., , Expeditious synthesis of phenanthrenes via CuBr2-catalyzed coupling of terminal alkynes and N-tosylhydrazones derived from O -formyl biphenyls Org. Lett. 13 , 5020-5023, (2011)
- 3. P. D. Thornton, et al., , Application of 6,7-Indole Aryne Cycloaddition and Pd(0)-Catalyzed Suzuki-Miyaura and Buchwald-Hartwig Cross-Coupling Reactions for the Preparation of Annulated Indole Libraries ACS Comb. Sci. 13 , 443-448, (2011) 摘要
- 4. H. Yang, et al., , General Copper-Catalyzed Transformations of Functional Groups from Arylboronic Acids in Water Chem. Eur. J. 17 , 5652-5660, (2011)
- 5. X. Zhang, et al., , Design, Synthesis, and Characterization of Crosslinkable Doped NLO Materials Based on Polyurethanes Containing Spindle-Type Chromophores Macromol. Chem. Phys. 212 , 879-886, (2011)
- Tetrahedron Asymmetry 14 , 3435-3446, (2003)
- D. A. DeGoey, et al., , P1-Substituted Symmetry-Based Human Immunodeficiency Virus Protease Inhibitors with Potent Antiviral Activity against Drug-Resistant Viruses J. Med. Chem. 54 , 7094-7104, (2011)
安全信息
- H315 Causes skin irritation 会刺激皮肤
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
- P302+P352
- P305+P351+P338
- P305+P351+P338+P337+P313
- P332+P313
- P362 Take off contaminated clothing and wash before reuse. 脱掉污染的衣服，清洗后方可重新使用
- S26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 眼睛接触后，立即用大量水冲洗并征求医生意见；
- S37 Wear suitable gloves 戴适当手套；
- S37/39 Wear suitable gloves and eye/face protection 穿戴适当的手套和眼睛/面保护；
- R36/37/38 Irritating to eyes, respiratory system and skin 对眼睛、呼吸系统和皮肤有刺激性
GHS Symbol
其他信息
- 水中溶解度:25 g/l。
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