CAS 5535-55-7
:1-(ethenylsulfonyl)-4-nitrobenzene
Description:
1-(Ethenylsulfonyl)-4-nitrobenzene, with the CAS number 5535-55-7, is an organic compound characterized by the presence of both a nitro group and a vinylsulfonyl group attached to a benzene ring. This compound typically appears as a solid at room temperature and is known for its reactivity due to the presence of the vinylsulfonyl moiety, which can participate in various chemical reactions, including nucleophilic additions and polymerization processes. The nitro group contributes to the compound's electron-withdrawing properties, influencing its reactivity and solubility in different solvents. It is often utilized in organic synthesis and may serve as an intermediate in the production of more complex molecules. Safety precautions should be observed when handling this compound, as it may pose health risks, including potential toxicity and environmental hazards. Proper storage conditions and protective equipment are recommended to mitigate any risks associated with its use.
Formula:C8H7NO4S
InChI:InChI=1/C8H7NO4S/c1-2-14(12,13)8-5-3-7(4-6-8)9(10)11/h2-6H,1H2
SMILES:C=CS(=O)(=O)c1ccc(cc1)N(=O)=O
Synonyms:- Benzene, 1- (ethenylsulfonyl)-4-nitro-
- p-Nitrophenyl vinyl sulfone
- Sulfone, p-nitrophenyl vinyl
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Found 1 products.
1-(Ethenesulfonyl)-4-nitrobenzene
CAS:1-(Ethenesulfonyl)-4-nitrobenzene (1ESNB) is a pyrazoline that has been used as an oxidant in cyclic aliphatic and heterocyclic syntheses. 1ESNB is also used to form phosphate derivatives, which are important in the pharmaceutical industry. 1ESNB can be prepared by the organocatalytic coupling of ethyl sulfone with nitrobenzene. The azomethine ylide can be generated from 1ESNB through oxidation with potassium permanganate or ozone, followed by addition of an aliphatic amine. This reaction gives a quinolinium salt that can be converted to a sulfone using thionyl chloride or oxalyl chloride. A cycloaddition reaction can then convert the sulfone into a biologically active molecule such as methotrexate or daunorubicin.
Formula:C8H7NO4SPurity:Min. 95%Molecular weight:213.21 g/mol
