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Merck
CN

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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关于此项目

线性分子式:
CF3C6H4SO2Cl
化学文摘社编号:
分子量:
244.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2113604
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产品名称

4-(三氟甲基)苯磺酰氯, 97%

InChI

1S/C7H4ClF3O2S/c8-14(12,13)6-3-1-5(2-4-6)7(9,10)11/h1-4H

SMILES string

FC(F)(F)c1ccc(cc1)S(Cl)(=O)=O

InChI key

OZDCZHDOIBUGAJ-UHFFFAOYSA-N

assay

97%

mp

30-34 °C (lit.)

functional group

fluoro

Quality Level

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Disclaimer

低熔点固体

Application

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.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

supp_hazards

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

>230.0 °F

flash_point_c

> 110 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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"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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