missing translation for 'onlineSavingsMsg'
Learn More
  1. Home
  2. Products
  3. Chemikalien
  4. Organische Verbindungen
  5. Benzoide
  6. Benzol und substituierte Derivate
  7. Hydroxybenzoesäurederivate
  8. O-Acetylsalicyloylchlorid, 97 %, Thermo Scientific Chemicals

O-Acetylsalicyloylchlorid, 97 %, Thermo Scientific Chemicals

Artikelnummer. 11364364
Change view
Click to view available options
Menge:
5 g
25 g
100 g
Packungsgröße:
100 Gramm
25 Gramm
5 Gramm
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Artikelnummer. Menge unitSize
11364364 5 g 5 Gramm
11374364 25 g 25 Gramm
11384364 100 g 100 Gramm
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
This item is not returnable. View return policy
Product Code. 11364364 Supplier Thermo Scientific Alfa Aesar Supplier No. L00919.06
Bulk oder benutzerdefiniertes Format anfordern

Please to purchase this item. Need a web account? Register with us today!

This item is not returnable. View return policy

Description

CAS: 5538-51-2 | C9H7ClO3 | 198.602 g/mol

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.

Anwendungen
O-Acetylsalicyloylchlorid wurde bei der Synthese von enantiomerisch reinen heteroorganischen Bidentat-Liganden verwendet, die auf einfachen achiralen Skeletten gebaut wurden und eine Aziridingruppe enthielten. Es wurde bei der allgemeinen Synthese von Acetoxybenzamiden verwendet. Es wurde bei der chemischen Synthese von 2,2,6,6-Tetramethyl-1-Piperidinyloxy(TEMPO)-Aspirin-Konjugat über Kondensationsreaktion mit 4-Hydroxy-TEMPO verwendet. Es wurde als Reagenz bei der Acylierung von Cyclobutendionen verwendet.

Löslichkeit
Löslich in Toluol. Es reagiert mit Wasser.

Hinweise
Feuchtigkeitsempfindlich. Unter trockenem Inertgas lagern. Nicht in der Nähe starker Basen aufbewahren.
TRUSTED_SUSTAINABILITY

Chemical Identifiers

CAS 5538-51-2
Summenformel C9H7ClO3
Molekulargewicht (g/mol) 198.602
MDL-Nummer MFCD00000663
InChI-Schlüssel DSGKWFGEUBCEIE-UHFFFAOYSA-N
Synonym 2-acetoxybenzoyl chloride, o-acetylsalicyloyl chloride, acetylsalicyloyl chloride, 2-chlorocarbonyl phenyl acetate, benzoyl chloride, 2-acetyloxy, aspirin chloride, o-acetylsalicyloylchloride, acetylsalicoyl chloride, 2-carbonochloridoyl phenyl acetate, ascc
PubChem CID 79668
IUPAC-Name (2-carbonochloridoylphenyl)acetat
SMILES CC(=O)OC1=CC=CC=C1C(=O)Cl

Specifications

Chemischer Name oder Material O-Acetylsalicyloyl chloride
Schmelzpunkt 47°C to 50°C
Siedepunkt 134°C to 136°C (12 mmHg)
Flammpunkt >110°C (230°F)
Geruch Pungent, Makes Eyes Water
Menge 5 g
UN-Nummer UN3261
Beilstein 880372
Formelmasse 198.61
Reinheit (%) 97%

RUO – Research Use Only

Product Title
Select an issue

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.