Weight | 102.089 g/mol |
---|---|
Formula | C4H6O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
ACETIC ANHYDRIDE (108-24-7)
acetic anhydride, 3H-labeled
Score:
#209 in Biochemistry
,
#325 in Physics
,
#925 in Chemistry
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- Femtomole sensitive radioimmunoassay for cyclic AMP and cyclic GMP after 2'0 acetylation by acetic anhydride in aqueous solution. (Journal of cyclic nucleotide research, 1975)
- Direct determination of citric acid in milk with an improved pyridine-acetic anhydride method. (Journal of Dairy Science, 1958)
- Cobalt(II) chloride catalyzed acylation of alcohols with acetic anhydride: scope and mechanism (Journal of Organic Chemistry, 1992)
- Influence of acetic anhydride on physicochemical, morphological and thermal properties of corn and potato starch (Food Chemistry, 2004)
- Acylation of alcohols with acetic anhydride catalyzed by TaCl5: Some implications in kinetic resolution (Tetrahedron Letters, 1998)
- THE OXIDATION OF 1,2;5,6-DI-O-ISOPROPYLIDENE-D-GLUCOSE BY DIMETHYL SULFOXIDE ACETIC ANHYDRIDE (Canadian Journal of Chemistry, 1966)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - H313: May be harmful in contact with skin
Acute toxicity, dermal - Category 5 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H318: Causes serious eye damage
Danger Serious eye damage/eye irritation - Category 1 - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - H402: Harmful to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 3 - acetic anhydride, 3H-labeled
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SMILESCC(=O)OC(=O)C
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InChIKeyWFDIJRYMOXRFFG-UHFFFAOYSA-N
- Pubchem - ACETIC ANHYDRIDE
- Wikipedia - acetic anhydride
Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH3CO)2O. Commonly abbreviated Ac2O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with moisture in the air.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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57-71-6
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ethyl acetoacetate
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Diisopropyl ether
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(543-27-1)
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