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Thermo Scientific Chemicals
Acetoxyacetyl chloride, 97%
CAS: 13831-31-7 | C4H5ClO3 | 136.531 g/mol
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Catalog number H25797.06
also known as H25797-06
Price (USD)
41.65
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Online exclusive
Ends: 30-Jun-2026
48.50Save 6.85 (14%)
Each
Quantity:
5 g
Price (USD)
41.65
Special offer
Online exclusive
Ends: 30-Jun-2026
48.50Save 6.85 (14%)
Each
Chemical Identifiers
CAS13831-31-7
IUPAC Name2-chloro-2-oxoethyl acetate
Molecular FormulaC4H5ClO3
InChI KeyHZDNNJABYXNPPV-UHFFFAOYSA-N
SMILESCC(=O)OCC(Cl)=O
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Specifications
Specification Sheet
Specification SheetRefractive Index1.4245-1.4295 @ 20°C (non-U.S. sourced material)
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥96.0%
CommentMaterial Sourced in the U.S. and in other countries
Acetoxyacetyl chloride was used in synthesis of stabilized axial and equatorial conformers of spiro-β-lactams and glycolylhydroxamic acids.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Acetoxyacetyl chloride was used in synthesis of stabilized axial and equatorial conformers of spiro-β-lactams and glycolylhydroxamic acids.
Solubility
Reacts with water violently.
Notes
Moisture sensitive. Store away from oxidizing agents, bases, water/ moisture.
Acetoxyacetyl chloride was used in synthesis of stabilized axial and equatorial conformers of spiro-β-lactams and glycolylhydroxamic acids.
Solubility
Reacts with water violently.
Notes
Moisture sensitive. Store away from oxidizing agents, bases, water/ moisture.
RUO – Research Use Only
General References:
- Hiromune Ando;, Yusuke Koike; Hideharu Ishida; Makoto Kiso. Extending the possibility of an N-Troc-protected sialic acid donor toward variant sialo-glycoside synthesis. Tetrahedron Letters. 2003, 44 (36), 6883-6886.
- OM Walsh; MJ Meegan; RM Prendergast; T Al Nakib. Synthesis of 3-acetoxyazetidin-2-ones and 3-hydroxyazetidin-2-ones with antifungal and antibacterial activity. European Journal of Medicinal Chemistry. 1996, 31 (12), 989-1000.