missing translation for 'onlineSavingsMsg'
Learn More

Oxalyl chloride, 2M soln. in dichloromethane

Product Code. 15464217
Change view
Click to view available options
Quantity:
100 mL
500 mL
Unit Size:
100mL
500mL
2 product options available for selection
Product selection table with 2 available options. Use arrow keys to navigate and Enter or Space to select.
Product Code. Quantity unitSize
15464217 500 mL 500mL
15454217 100 mL 100mL
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 2 options available.
2 options
Les retours ne sont pas autorisés pour ce produit. Afficher la politique du retour.
Règlementaire: Ce produit est un intermédiaire isolé transporté conformément au règlement (CE) 1907/2006 (REACH). tout client doit remplir une déclaration avant la livraison.
Code produit. 15464217 missing translation for 'mfr' Thermo Scientific Alfa Aesar missing translation for 'supplierNo' H31617.AP
 Restricted Item
Estimated Shipment: 20-08-2026
Ajouter au panier
Ajouter au panier
Request Bulk or Custom Format
Les retours ne sont pas autorisés pour ce produit. Afficher la politique du retour.
Règlementaire: Ce produit est un intermédiaire isolé transporté conformément au règlement (CE) 1907/2006 (REACH). tout client doit remplir une déclaration avant la livraison.

CAS: 79-37-8 | C2Cl2O2 | 126.92 g/mol

Reagent used in organic synthesis. Unncatalyzed reaction of silyl ketene acetals with oxalyl chloride yeilds symmetrical pulvinic acids. Catalytic syntheses of N-heterocyclic ynones and ynediones by in situ activation of carboxylic acids with oxalyl chloride. Oxalyl chloride was reportedly used in the first synthesis of dioxane tetraketone.

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
Reagent used in organic synthesis. Unncatalyzed reaction of silyl ketene acetals with oxalyl chloride yeilds symmetrical pulvinic acids. Catalytic syntheses of N-heterocyclic ynones and ynediones by in situ activation of carboxylic acids with oxalyl chloride. Oxalyl chloride was reportedly used in the first synthesis of dioxane tetraketone.

Solubility
Reacts with water.

Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture, light, bases, alkali metals, alcohols, dimethyl formamide.
TRUSTED_SUSTAINABILITY

Identifiants chimiques

CAS 79-37-8
Molecular Formula C2Cl2O2
Molecular Weight (g/mol) 126.92
MDL Number MFCD00000704
InChI Key CTSLXHKWHWQRSH-UHFFFAOYSA-N
Synonym oxalyl chloride, ethanedioyl dichloride, oxalic dichloride, oxaloyl chloride, oxalic acid dichloride, oxalic acid chloride, ethanedioyl chloride, oxalylchloride, unii-r4y96317dw, cocl 2
PubChem CID 65578
IUPAC Name oxalyl dichloride
SMILES C(=O)(C(=O)Cl)Cl

Spécification

Density 1.335
Quantity 500 mL
UN Number UN2922
Sensitivity Moisture sensitive
Solubility Information Reacts with water.
Formula Weight 126.93
Concentration or Composition (by Analyte or Components) 2M soln. in dichloromethane
Chemical Name or Material Oxalyl chloride

RUO – Research Use Only

Nom du produit
Sélectionnez un problème

En cliquant sur Soumettre, vous reconnaissez que vous pouvez être contacté par Fisher Scientific au sujet des informations que vous avez fournies dans ce formulaire. Nous ne partagerons pas vos informations à d'autres fins. Toutes les informations de contact fournies seront également conservées conformément à notre politique de confidentialité. Politique de confidentialité.