O-Acetylsalicyloyl Chloride

CAS: 5538-51-2

Ref. TR-A187935

Produktinformation

• Name: O-Acetylsalicyloyl Chloride
• Synonyme: 2-(Acetyloxy)benzoyl Chloride, Salicyloyl Chloride Acetate, 2-(Acetyloxy)benzoyl Chloride, 2-(Chlorocarbonyl)phenyl Acetate, 2-Acetoxybenzoyl Chloride, 2-Acetylsalicyloyl Chloride, Acetic Acid 2-Chlorocarbonylphenyl Ester, Acetoxybenzoic Acid Chloride, Acetylsalicyl Chloride, Acetylsalicylic Acid Chloride, Acetylsalicyloyl Chloride, Aspiryl Chloride, NSC 97216, O-Acetylsalicylic Acid Chloride, o-(Acetyloxy)benzoyl Chloride, o-Acetoxybenzoyl Chloride, 2-(Acetyloxy)benzoyl chloride, 2-(Carbonochloridoyl)phenyl acetate, 2-(Chlorocarbonyl)Phenyl Acetate, 2-Acetylsalicyloyl chloride, Acetic acid 2-chlorocarbonylphenyl ester, Acetoxybenzoic acid chloride, Acetylsalicyl chloride, Acetylsalicylic acid chloride, Acetylsalicyloyl chloride, Aspirin acyl chloride, Aspirinyl chloride, Aspiryl chloride, Benzoyl chloride, 2-(acetyloxy)-, O-Acetylsalicylic acid chloride, O-Acetylsalicyloyl chloride, Salicyloyl chloride, acetate, o-(Acetyloxy)benzoyl chloride, o-Acetoxybenzoyl chloride

Beschreibung

Stability Moisture Sensitive
Applications O-Acetylsalicyloyl chloride is used in the derivatisation of amines, and also improve electrochemical detection of these amines when they are run through high-performance liquid chromatography. O-Acetylsalicyloyl chloride is also used as a reagent to synthesize benzimidazole derivatives, compounds that inhibit leukotriene synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Banoglu, E., et al.: Bioorg. Med. Chem., 20, 3728 (2012); Smith, R., et al.: J. Chromatogr. A, 455, 349 (1988)

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 198.6
• Formel: C₉H₇ClO₃
• Farbe/Form: Neat
• InChl: InChI=1S/C9H7ClO3/c1-6(11)13-8-5-3-2-4-7(8)9(10)12/h2-5H,1H3
• InChI Key: InChIKey=DSGKWFGEUBCEIE-UHFFFAOYSA-N
• SMILES: CC(=O)Oc1ccccc1C(=O)Cl