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| METHYL OXALYL CHLORIDE Basic information | | Uses |
| Product Name: | METHYL OXALYL CHLORIDE | | Synonyms: | MONO-METHYL OXALYL CHLORIDE;CHLOROGLYOXYLIC ACID METHYL ESTER;METHYL CHLOROFORMYLFORMATE;METHYL CHLOROGLYOXALATE;METHYL CHLOROGLYOXYLATE;METHYL CHLOROOXOACETATE;METHYL OXALYL CHLORIDE;Methyl Oxalyl Choride | | CAS: | 5781-53-3 | | MF: | C3H3ClO3 | | MW: | 122.51 | | EINECS: | 227-307-4 | | Product Categories: | Organics | | Mol File: | 5781-53-3.mol |
| METHYL OXALYL CHLORIDE Chemical Properties |
| Boiling point | 118-120 °C (lit.) | | density | 1.332 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.419(lit.) | | Fp | 116 °F | | storage temp. | Inert atmosphere,2-8°C | | form | Liquid | | color | Clear | | Water Solubility | Miscible with water. | | Sensitive | Moisture Sensitive | | BRN | 1071541 | | InChIKey | ZXUQEPZWVQIOJE-UHFFFAOYSA-N | | CAS DataBase Reference | 5781-53-3(CAS DataBase Reference) | | EPA Substance Registry System | Acetic acid, chlorooxo-, methyl ester (5781-53-3) |
| METHYL OXALYL CHLORIDE Usage And Synthesis |
| Uses | Methyl oxalyl chloride is an important organic intermediate (building block) to synthetize substituted methyl oxalyl products. It can be used for regioselective synthesis of fused coumarins, cyclization to form substituted isoxazoles and heterocycles, intramolecular Wittig reactions, silyl enol ether acylation, and iron-mediated cleavage of C-C bonds.
| | Chemical Properties | CLEAR LIQUID | | Uses | Methyl oxalyl chloride is used as a synthetic reagent. It serves as a reagent in the synthesis of fused coumarins, substituted isoxazoles and heterocycles. Further, it is used in intramolecular Wittig reactions, and iron-mediated cleavage of C-C bonds. | | Uses | Reactant involved in:- Regioselective synthesis of fused coumarins
- Cyclization to form substituted isoxazoles and heterocycles
- Intramolecular Wittig reactions
- Silyl enol ether acylation
- Iron-mediated cleavage of C-C bonds
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| METHYL OXALYL CHLORIDE Preparation Products And Raw materials |
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