CAS 5781-53-3
:Methyl oxalyl chloride
Description:
Methyl oxalyl chloride, with the CAS number 5781-53-3, is an organic compound characterized by its structure, which includes a methyl group and two oxalyl chloride functional groups. It is a colorless to pale yellow liquid that is known for its strong reactivity, particularly as a chlorinating agent. This compound has a pungent odor and is highly corrosive, necessitating careful handling and storage in a well-ventilated area with appropriate personal protective equipment. Methyl oxalyl chloride is soluble in organic solvents but reacts vigorously with water, releasing hydrochloric acid and forming methyl oxalate. It is primarily used in organic synthesis, particularly in the preparation of various chemical intermediates and in the production of pharmaceuticals and agrochemicals. Due to its reactivity, it poses significant health hazards, including respiratory irritation and potential skin burns, making it essential to follow safety protocols when working with this substance.
Formula:C3H3ClO3
InChI:InChI=1S/C3H3ClO3/c1-7-3(6)2(4)5/h1H3
InChI key:InChIKey=ZXUQEPZWVQIOJE-UHFFFAOYSA-N
SMILES:C(C(Cl)=O)(OC)=O
Synonyms:- (Chloro)(oxo)acetic acid methyl ester
- Acetic acid, 2-chloro-2-oxo-, methyl ester
- Acetic acid, chlorooxo-, methyl ester
- Chloroglyoxylic acid methyl ester
- Glyoxylic acid, chloro-, methyl ester
- Methoxalyl chloride
- Methoxyoxalyl chloride
- Methyl (chlorocarbonyl)formate
- Methyl (chloroformyl)formate
- Methyl 2-chloro-2-oxoacetate
- Methyl Chlorooxoacetate
- Methyl chloroglyoxylate
- Methyl chlorooxalate
- Monomethyl oxalate chloride
- Monomethyl oxalate monochloride
- Monomethyl oxalyl chloride
- Oxalic acid methyl ester chloride
- Oxalic acid monomethyl ester chloride
- See more synonyms
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Found 8 products.
Methyl Chloroglyoxylate
CAS:Formula:C3H3ClO3Purity:>98.0%(GC)(T)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:122.50Methyl oxalyl chloride, 97%
CAS:<p>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. This Thermo Scientific Chemicals brand product </p>Formula:C3H3ClO3Purity:97%Color and Shape:Clear colorless, LiquidMolecular weight:122.50Methyl chlorooxoacetate
CAS:Formula:C3H3ClO3Purity:98%Color and Shape:LiquidMolecular weight:122.5071Methyl oxalyl chloride
CAS:Formula:C3H3ClO3Purity:≥ 98.0%Color and Shape:Colourless to light-yellow liquidMolecular weight:122.51METHYL (CHLOROCARBONYL)FORMATE
CAS:Formula:C3H3ClO3Purity:97.0%Color and Shape:LiquidMolecular weight:122.5Methyl Chlorooxoacetate
CAS:Controlled Product<p>Applications Methyl Chlorooxoacetate is used as a reagent in organic synthesis of several compounds including that of coumarin-based probes which fluoresce in response to detection of Pi in cell culture and Caenorhabditis elegans. Also used in the synthesis of phenanthrene β-diketo acids which is being studied as potential HIV-1 integrase inhibitors.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Wang, H., et al.: Dyes Pigments, 120, 293 (2015); Sharma, H., et al.: Bioorg. Med. Chem. Lett., 23, 6146 (2013);<br></p>Formula:C3H3ClO3Color and Shape:NeatMolecular weight:122.51Methyl chlorooxoacetate
CAS:<p>Methyl chlorooxoacetate is an oxalyl ester that has been used for the synthesis of glycol esters. Methyl chlorooxoacetate has been shown to have a high solubility in water and organic solvents, which is desirable for industrial processes. This molecule also has the ability to be acylated with various organic groups and can act as a process-optimization agent in plant physiology. Methyl chlorooxoacetate binds as a receptor to growth factors and HIV infection, which leads to amide formation and carbonyl group formation.</p>Formula:C3H3ClO3Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:122.51 g/mol







