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O-Acetylsalicyloyl chloride, 97%, Thermo Scientific Chemicals
Catalog number: L00919.22
100 g, Each
Thermo Scientific Chemicals
O-Acetylsalicyloyl chloride, 97%, Thermo Scientific Chemicals
Catalog number: L00919.22
100 g, Each
Quantity
Catalog number: L00919.22
also known as L00919-22
Price (USD)
329.00
Each
Quantity
-
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Chemical Identifiers
CAS
5538-51-2
IUPAC Name
2-(carbonochloridoyl)phenyl acetate
Molecular Formula
C9H7ClO3
InChI Key
DSGKWFGEUBCEIE-UHFFFAOYSA-N
SMILES
CC(=O)OC1=CC=CC=C1C(Cl)=O
Specifications
Specification SheetAppearance (Color)
White to cream to yellow or pale pink
Form
Crystals or powder or crystalline powder or lumps or chunks or fused solid or granules or clear liquid as melt
Assay (Titration ex Chloride)
≥96.0 to ≤104.0%
Melting Point (clear melt)
45.0-54.0?C
Refractive Index
1.5340-1.5390 @ 20?C
Description
O-Acetylsalicyloyl chloride was used in the synthesis of enantiomerically pure bidentate heteroorganic ligands built on simple achiral skeletons and containing an aziridine moiety. It was used in the general synthesis of acetoxybenzamides. It was used in the chemical synthesis of 2,2,6,6-tetramethyl-1-piperidinyloxy(TEMPO)-aspirin conjugate via condensation reaction with 4-hydroxy-TEMPO. It was used as reagent in acylation of cyclobutenediones.
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
O-Acetylsalicyloyl chloride was used in the synthesis of enantiomerically pure bidentate heteroorganic ligands built on simple achiral skeletons and containing an aziridine moiety. It was used in the general synthesis of acetoxybenzamides. It was used in the chemical synthesis of 2,2,6,6-tetramethyl-1-piperidinyloxy(TEMPO)-aspirin conjugate via condensation reaction with 4-hydroxy-TEMPO. It was used as reagent in acylation of cyclobutenediones.
Solubility
Soluble in toluene. Reacts with water.
Notes
Moisture Sensitive. Store under dry inert gas. Store away from strong bases.
O-Acetylsalicyloyl chloride was used in the synthesis of enantiomerically pure bidentate heteroorganic ligands built on simple achiral skeletons and containing an aziridine moiety. It was used in the general synthesis of acetoxybenzamides. It was used in the chemical synthesis of 2,2,6,6-tetramethyl-1-piperidinyloxy(TEMPO)-aspirin conjugate via condensation reaction with 4-hydroxy-TEMPO. It was used as reagent in acylation of cyclobutenediones.
Solubility
Soluble in toluene. Reacts with water.
Notes
Moisture Sensitive. Store under dry inert gas. Store away from strong bases.
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