Methacryloyl Chloride
- CAS No.
- 920-46-7
Methacryloyl Chloride, CAS 920-46-7. Source-derived identification, physical data and applications are provided for catalogue reference; request the current specification, COA and SDS for the…
GTC-202

Acyl Halides
Allyl Chlorooxalate, CAS 74503-07-4. Source-derived identification, physical data and applications are provided for catalogue reference; request the current specification, COA and SDS for the required grade.
Allyl oxalyl chloride; Allyl 2-chloro-2-oxoacetate; 2-Propen-1-yloxy chloroacetate; Chlorooxoacetic acid 2-propenyl ester; prop-2-enyl 2-chloro-2-oxoacetate; Allyl chlorooxoacetate; Oxalic acid monoallyl ester chloride
Supplied catalogue source: GTC-202 · Page 13
The information below is a structured migration from the supplied catalogue snapshot. It is not a current product specification, COA or SDS. Confirm the actual supplier, grade, batch documents, classification, packing and destination requirements for your enquiry.
Allyl chlorooxalate is a reactive liquid ester-acid chloride that combines allyl and oxalyl functionalities, making it valuable for selective acylation and cross-coupling reactions in complex molecule synthesis. It is particularly important in the construction of beta-lactam frameworks found in modern antibiotics. The compound's dual reactivity demands careful handling under inert or controlled conditions to maintain stability and prevent decomposition.
| CAS No. | 74503-07-4 |
|---|---|
| EC No. | 277-900-7 |
| Linear Formula | CH2=CHCH2OC(O)C(O)Cl |
| Molecular Weight | 148.54 g/mol |
| Appearance | Liquid |
| Melting Point | Not available (lit.) |
| Boiling point | 50-51 °C at 12 Torr (lit.) |
| Density | 1.213 g/mL at 25 °C (lit.) |
| RIDADR | UN 2920 Class 3 (8) PG II |
| Chemical Structure | ![]() |
Pharmaceutical intermediate for penem antibiotics: Allyl chlorooxalate is a key building block in the industrial synthesis of Sulopenem and other penem-class antibiotics used for treating resistant bacterial infections.
Reactive acylating agent in synthesis: It functions as an effective reagent for introducing allyloxalyl or related functional groups during the preparation of complex pharmaceutical intermediates and fine chemicals.
Specialty chemical and API production: Employed in the manufacture of active pharmaceutical ingredients and advanced intermediates requiring precise oxalyl or ester modifications.
Organic synthesis applications: Used in research and development laboratories for constructing functionalized molecules in medicinal chemistry and materials science projects.
Custom synthesis and contract manufacturing: Serves as a versatile starting material for custom synthesis routes in the pharmaceutical and specialty chemical industries.
High purity specifications and strict batch consistency: Our allyl chlorooxalate is manufactured and tested to meet the exacting standards required for pharmaceutical intermediate applications and sensitive synthetic processes.
Complete SDS, COA and dangerous goods documentation available: Comprehensive regulatory documentation including safety data sheets and certificates of analysis supports compliance for international transport and procurement of this reactive material.
GHS Classification: Flammable liquids (Category 3) GHS02; Skin corrosion (Category 1B) GHS05; Acute toxicity, oral (Category 4) GHS07.
Hazard Statements: H226 - Flammable liquid and vapour. H314 - Causes severe skin burns and eye damage. H302 - Harmful if swallowed.
UN Number: UN 2920 | Hazard Class: 3 (Flammable liquid) subsidiary risk 8 (Corrosive) | Packing Group: II

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