3-碘苯酚
外观
3-碘苯酚 | |
---|---|
IUPAC名 3-Iodophenol 3-碘苯酚 | |
别名 | 间碘苯酚 3-羟基碘苯 |
识别 | |
CAS号 | 626-02-8 |
PubChem | 12272 |
ChemSpider | 11769 |
SMILES |
|
InChI |
|
InChIKey | FXTKWBZFNQHAAO-UHFFFAOYSA-N |
ChEBI | 33439 |
性质 | |
化学式 | C6H5IO |
摩尔质量 | 220.01 g·mol−1 |
熔点 | 118 °C(244 °F;391 K)[1] |
沸点 | 186 °C(367 °F;459 K)(100 mmHg)[1] |
pKa | 9.03[2] |
危险性 | |
GHS危险性符号 | |
GHS提示词 | 警告 |
H-术语 | H315, H319, H335 |
P-术语 | P261, P305+351+338 |
相关物质 | |
相关化学品 | |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
3-碘苯酚或间碘苯酚,是一种芳香族有机化合物。3-碘苯酚参与各种偶联反应,其中碘取代基被置换。[3]被广泛引用的例子包括硫醇盐[4]和胺亲核试剂。[5]
- IC
6H
4CO
2H + "O" → IC
6H
4OH + CO
2
参考资料
[编辑]- ^ 1.0 1.1 Haynes 2016,第3.324頁.
- ^ Haynes 2016,第5.93頁.
- ^ 3-Iodophenol. Fisher Scientific. [2023-04-28]. (原始内容存档于2023-05-01).
- ^ Kwong, Fuk Yee; Buchwald, Stephen L. A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols. Organic Letters. 2002, 4 (20): 3517–3520. PMID 12323058. doi:10.1021/ol0266673.
- ^ Shen, Qilong; Ogata, Tokutaro; Hartwig, John F. Highly Reactive, General and Long-Lived Catalysts for Palladium-Catalyzed Amination of Heteroaryl and Aryl Chlorides, Bromides, and Iodides: Scope and Structure–Activity Relationships. Journal of the American Chemical Society. 2008, 130 (20): 6586–6596. PMC 2822544 . PMID 18444639. doi:10.1021/ja077074w.
- ^ Xiong, Wenzhang; Shi, Qiu; Liu, Wenbo H. Simple and Practical Conversion of Benzoic Acids to Phenols at Room Temperature. Journal of the American Chemical Society. 2022, 144 (34): 15894–15902. PMID 35997485. S2CID 251742827. doi:10.1021/jacs.2c07529.
参考书目
[编辑]- Haynes, William M. (编). CRC Handbook of Chemistry and Physics 97th. CRC Press. 2016. ISBN 9781498754293.
这是一篇有机化学小作品。您可以通过编辑或修订扩充其内容。 |