硅烷化
二氟卡宾
化学
烯醇
亲核细胞
苯
无水的
甲苯
溶解度
乙腈
重氮甲烷
反应性(心理学)
有机化学
药物化学
催化作用
替代医学
病理
医学
标识
DOI:10.1002/047084289x.rn01019
摘要
[384-67-8] C8H5ClF2O (MW 190.56)
InChI = 1S/C8H5ClF2O/c9-8(10,11)7(12)6-4-2-1-3-5-6/h1-5H
InChIKey = MNOONJNILVDLSW-UHFFFAOYSA-N
(precursor for the preparation of 2,2-difluoro enol silyl ethers or 2,2-difluoro enol silyl phosphates;9-12 difluorocarbene precursor;6 precursor for the synthesis of gem-difluoromethene-containing compounds13-22)
Physical Data: colorless liquid; bp 84–85 °C/25 mmHg.1
Solubility: sol alcohols, ethers, CH2Cl2, CHCl3, benzene, toluene, acetonitrile, DMF, and DMSO.
Form Supplied in: colorless liquid; often prepared by the reaction between chlorodifluoroacetic acid and PhMgBr,2-5 or prepared by chlorination of [2,2-difluoro-1-[(trimethylsilyl)oxy]ethenyl]benzene.6
Handling, Storage, and Precautions: 2-chloro-2,2-difluoroacetophenone (PhCOCF2Cl) has high reactivity with bases, nucleophiles, reducing agents, and single-electron transferring agent; store under anhydrous, neutral conditions; use in a fume hood.
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