| Weight | 126.926 g/mol |
|---|---|
| Formula | C2Cl2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Oxalyl chloride (79-37-8)
Score:
#1931 in Physics
,
#6042 in Chemistry
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- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride (Journal of Organic Chemistry, 1978)
- Structure of the dimethyl sulfoxide-oxalyl chloride reaction product. Oxidation of heteroaromatic and diverse alcohols to carbonyl compounds (Journal of Organic Chemistry, 1979)
- THE ACTION OF OXALYL CHLORIDE ON INDOLES: A NEW APPROACH TO TRYPTAMINES (Journal of the American Chemical Society, 1954)
- THE USE OF OXALYL CHLORIDE AND BROMIDE FOR PRODUCING ACID CHLORIDES, ACID BROMIDES OR ACID ANHYDRIDES. III. (Journal of the American Chemical Society, 1920)
- Reaction of tert-butyldimethylsilyl esters with oxalyl chloride-dimethylformamide: preparation of carboxylic acid chlorides under neutral conditions (Journal of Organic Chemistry, 1978)
- The Reaction of Oxalyl Chloride with Amides. II. Oxazolidinediones and Acyl Isocyanates (Journal of Organic Chemistry, 1963)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=O)(C(=O)Cl)Cl
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InChIKeyCTSLXHKWHWQRSH-UHFFFAOYSA-N
- Pubchem - Oxalyl chloride
- Wikipedia - oxalyl chloride
Oxalyl chloride is a chemical compound with the formula (COCl)2. This colourless, sharp-smelling liquid, the diacid chloride of oxalic acid, is a useful reagent in organic synthesis. It can be prepared by treating oxalic acid with phosphorus pentachloride.
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Oxalyl chloride
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