F6206
4-氟苯磺酰氯
98%
别名:
4-氟苯磺酰氯, 对氟苯磺酰氯
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关于此项目
线性分子式:
FC6H4SO2Cl
化学文摘社编号:
分子量:
194.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-493-0
Beilstein/REAXYS Number:
2091633
MDL number:
Assay:
98%
产品名称
4-氟苯磺酰氯, 98%
InChI
1S/C6H4ClFO2S/c7-11(9,10)6-3-1-5(8)2-4-6/h1-4H
InChI key
BFXHJFKKRGVUMU-UHFFFAOYSA-N
SMILES string
Fc1ccc(cc1)S(Cl)(=O)=O
assay
98%
bp
95-96 °C/2 mmHg (lit.)
mp
29-31 °C (lit.)
Quality Level
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signalword
Danger
hcodes
Hazard Classifications
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
Y A Chang et al.
Bioconjugate chemistry, 3(2), 200-202 (1992-03-01)
4-Fluorobenzenesulfonyl chloride (fosyl chloride), due to the strong electron-withdrawing property of its fluoride atom, is found to be an excellent activating agent for the covalent attachment of biologicals to a variety of solid supports (e.g. functionalized polystyrene microspheres, Sepharose beads
Umaprasana Ojha et al.
Langmuir : the ACS journal of surfaces and colloids, 25(11), 6319-6327 (2009-04-02)
Peptide surface modification of poly[(methyl methacrylate-co-hydroxyethyl methacrylate)-b-isobutylene-b-(methyl methacrylate-co-hydroxyethyl methacrylate)] P(MMA-co-HEMA)-b-PIB-b-P(MMA-co-HEMA) triblock copolymers with different HEMA/MMA ratios has been accomplished using an efficient synthetic procedure. The triblock copolymers were reacted with 4-fluorobenzenesulfonyl chloride (fosyl chloride) in pyridine to obtain the activated
T H Liao et al.
Analytical biochemistry, 148(2), 365-375 (1985-08-01)
The reagent p-fluorobenzenesulfonyl chloride modifies the protein side chains of tyrosine, lysine, and histidine and the alpha-NH2 group. The p-fluorobenzenesulfonyl (Fbs-) group, identified by the 19F nuclear magnetic resonance signal, exhibits a different 19F chemical shift for each functional group
Ning Li et al.
European journal of medicinal chemistry, 155, 531-544 (2018-06-18)
Ten novel symmetric 3,5-bis(arylidene)-4-piperidone derivatives (BAPs, 1-10) and fourteen dissymmetric BAPs (11-24) were synthesized and evaluated the cytotoxicity. All of the compounds have been screened for their anti-inflammatory activity characterized by evaluating their inhibitory effects on LPS-induced IL-6, TNF-α secretion.
Abdelaziz Houmam et al.
Physical chemistry chemical physics : PCCP, 14(1), 113-124 (2011-09-15)
Important aspects of the electrochemical reduction of a series of substituted arene sulfonyl chlorides are investigated. An interesting autocatalytic mechanism is encountered where the starting material is reduced both at the electrode and through homogeneous electron transfer from the resulting
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