| Weight | 189.041 g/mol |
|---|---|
| Formula | C8H6Cl2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
2,2-Dichloroacetophenone (2648-61-5)
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- Sigma-Aldrich - 2,2-Dichloroacetophenone95.50 USD
- Fisher Scientific - Search for 2,2-Dichloroacetophenone
- TCI - 2,2-Dichloroacetophenone74.00 USD
- Glutathione-dependent reductive dehalogenation of 2,2,4-trichloroacetophenone to 2,4-dichloroacetophenone (Biochemical Pharmacology, 1982)
- Experimental thermochemical study of 2-chloroacetophenone and 2,4-dichloroacetophenone (The Journal of Chemical Thermodynamics, 2014)
- Reaction of 2,2-dichloroacetophenone and benzaldehydes under conditions of the darzens condensation (Russian Chemical Bulletin, 1992)
- Method for the preparation of 4'-(substituted)-amino-2-(substituted) amino-3',5'-dichloroacetophenone and salts thereof (1989)
- ChemInform Abstract: THE DEBROMINATION OF ALPHA-BROMODERIVATIVES OF 2,4-DICHLOROACETOPHENONE BY DIETHYL PHOSPHITE (ChemInform, 1975)
- Rearrangement of enol acetates of -(3,5-dimethyl-1,2,4-triazol-1-yl)-2,4-dichloroacetophenone and -(1,2,4-triazol-1-yl)-2,4-dichloropropiophenone (Russian Chemical Bulletin, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(=O)C(Cl)Cl
-
InChIKeyCERJZAHSUZVMCH-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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2,2-Dichloroacetophenone
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