Weight | 120.579 g/mol |
---|---|
Formula | C5H9ClO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Pivaloyl chloride (3282-30-2)
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- Sigma-Aldrich - Pivaloyl chloride18.80 - 60.50 USD
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- REGIOSELECTIVE ACYLATION OF HEXOPYRANOSIDES WITH PIVALOYL CHLORIDE (Journal of Organic Chemistry, 1998)
- Amino-acids and peptides. XXXVI. Pivaloyl chloride as a reagent in the mixed anhydride synthesis of peptides (Collection of Czechoslovak Chemical Communications, 1962)
- Pivaloyl chloride/DMF: a new reagent for conversion of alcohols to chlorides (Tetrahedron Letters, 2010)
- Generation of N-acylpyridinium ions from pivaloyl chloride and pyridine derivatives by means of silyl triflates (Journal of Organic Chemistry, 2000)
- Beckmann rearrangement of oximes using pivaloyl chloride/DMF complex (Tetrahedron Letters, 2011)
- Reaction of pivaloyl chloride with internucleosidic hphosphonate diesters (Recueil des Travaux Chimiques des Pays-Bas, 1986)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 -
SMILESCC(C)(C)C(=O)Cl
-
InChIKeyJVSFQJZRHXAUGT-UHFFFAOYSA-N
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