InChI key
SEWNAJIUKSTYOP-UHFFFAOYSA-N
InChI
1S/C6H3Cl2NO4S/c7-5-2-1-4(14(8,12)13)3-6(5)9(10)11/h1-3H
SMILES string
[O-][N+](=O)c1cc(ccc1Cl)S(Cl)(=O)=O
assay
96%
form
powder
mp
59-60 °C (lit.)
Application
4-氯-3-硝基苯磺酰基氯化物可用于：
- 在通过铜催化的芳基化环化制备官能化的1H-茚中。
- 作为合成N芳基磺酰基-3-酰基吲哚芳基羰基腙衍生物的前体，其显示出潜在的杀线虫活性。
- 作为合成ferrostatin-1（fer-1）磺酰胺类似物的关键起始原料，它具有良好铁死亡抑制特性。
- 在4-氯-3-硝基苯硫醇的合成中。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Novel ferroptosis inhibitors with improved potency and ADME properties.
Hofmans, Sam et al.
Journal of Medicinal Chemistry, 59(5), 2041-2053 (2016)
A simple, fast and chemoselective method for the preparation of arylthiols.
Bellale, Eknath V et al.
Synthesis, 2009(19), 3211-3213 (2009)
Synthesis and quantitative structure-activity relationship (QSAR) study of novel N-arylsulfonyl-3-acylindole arylcarbonyl hydrazone derivatives as nematicidal agents.
Che, Zhiping et al.
Journal of Agricultural and Food Chemistry, 61(24), 5696-5705 (2013)
Xiaoming Zeng et al.
Journal of the American Chemical Society, 133(44), 17638-17640 (2011-10-13)
A variety of polysubstituted 1H-indenes can be prepared through the copper-catalyzed arylative cyclization of simple arylalkynes with commercially available aromatic sulfonyl chlorides that function as an aryl group donor. The reaction tolerates a broad range of functional groups, including bromide
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