| Weight | 190.651 g/mol |
|---|---|
| Formula | C7H7ClO2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Chloromethyl phenyl sulfone (7205-98-3)
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- Asymmetric Darzens reaction utilizing chloromethyl phenyl sulfone under phase-transfer catalyzed conditions (Tetrahedron, 2002)
- Specific ortho orientation in the vicarious substitution of hydrogen in aromatic nitro compounds with carbanion of chloromethyl phenyl sulfone (Tetrahedron, 1984)
- Vicarious Nucleophilic Substitution of Hydrogen and Formation of Aziridine Rings in Reactions of Benzonaphthyridines and their N-Oxides with Chloromethyl Phenyl Sulfone (Monatshefte Fur Chemie, 2001)
- Regioselectivity in SNH reactions of some 3-nitro-1,8-naphthyridines with chloromethyl phenyl sulfone (Journal of Heterocyclic Chemistry, 1991)
- Reactions of chloromethyl phenyl sulfone carbanion with nitrobenzophenones. The vicarious substitution of hydrogen versus the Darzens condensation (Chemistry Letters, 1984)
- Regioselectivity in SNH reactions of some 3-nitro-1,5-naphthyridines with chloromethyl phenyl sulfone (Canadian Journal of Chemistry, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)S(=O)(=O)CCl
-
InChIKeyNXAIQSVCXQZNRY-UHFFFAOYSA-N
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