产品名称
4-氯-3-硝基苯磺酰氯, 96%
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
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Synthesis and quantitative structure-activity relationship (QSAR) study of novel N-arylsulfonyl-3-acylindole arylcarbonyl hydrazone derivatives as nematicidal agents.
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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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