565849
4-(三氟甲基)苯磺酰氯
97%
别名:
α,α,α-Trifluoro-p-toluenesulfonyl chloride, 4-(Trifluoromethyl)benzene-1-sulfonyl chloride, [4-(Trifluoromethyl)phenyl]sulfonyl chloride, [p-(Trifluoromethyl)phenyl]sulfonyl chloride, p-Trifluoromethylbenzenesulfonyl chloride
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所有图片(2)
About This Item
线性分子式:
CF3C6H4SO2Cl
CAS号:
分子量:
244.62
Beilstein:
2113604
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
检测方案
97%
mp
30-34 °C (lit.)
SMILES字符串
FC(F)(F)c1ccc(cc1)S(Cl)(=O)=O
InChI
1S/C7H4ClF3O2S/c8-14(12,13)6-3-1-5(2-4-6)7(9,10)11/h1-4H
InChI key
OZDCZHDOIBUGAJ-UHFFFAOYSA-N
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应用
4-(Trifluoromethyl)benzenesulfonyl chloride may be used to synthesize β-arylated thiophenes and 2,5-diarylated pyrrolevia palladium catalyzed desulfitative arylation of thiophenes and pyrroles, respectively.
4-(Trifluoromethyl)benzenesulfonyl chloride and N-vinylpyrrolidinone in acetonitrile can undergo photo-irradiation with visible light in the presence of Ir(ppy)2(dtbbpy)PF6 ([4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis[2-(2-pyridinyl-N)phenyl-C]iridium(III)hexafluorophosphate) and disodium phosphate to give the corresponding E-vinyl sulfone.
4-(Trifluoromethyl)benzenesulfonyl chloride and N-vinylpyrrolidinone in acetonitrile can undergo photo-irradiation with visible light in the presence of Ir(ppy)2(dtbbpy)PF6 ([4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis[2-(2-pyridinyl-N)phenyl-C]iridium(III)hexafluorophosphate) and disodium phosphate to give the corresponding E-vinyl sulfone.
注意
低熔点固体
警示用语：
Danger
危险声明
危险分类
Skin Corr. 1B
补充剂危害
WGK
WGK 3
闪点(°F)
>230.0 °F
闪点(°C)
> 110 °C
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
"C-H Functionalization of Enamides: Synthesis of ?-Amidovinyl Sulfones via Visible-Light Photoredox Catalysis"
Jiang H, et al.
Advanced Synthesis & Catalysis, 355(4), 809-813 (2013)
"Benzenesulfonyl chlorides: new reagents for access to alternative regioisomers in palladium-catalysed direct arylations of thiophenes"
Yuan K, et al.
Chemical Science, 5(1), 392-396 (2014)
Palladium-Catalysed Direct Desulfitative Arylation of Pyrroles using Benzenesulfonyl Chlorides as Alternative Coupling Partners.
Jin R, et al.
Advanced Synthesis & Catalysis, 356(18), 3831-3841 (2014)
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