CAS 5781-53-3
:Cloruro de metiloxalilo
Descripción:
Cloruro de metiloxalilo, con el número CAS 5781-53-3, es un compuesto orgánico caracterizado por su estructura, que incluye un grupo metilo y dos grupos funcionales de cloruro de oxalilo. Es un líquido incoloro a amarillo pálido que se conoce por su fuerte reactividad, particularmente como agente clorante. Este compuesto tiene un olor penetrante y es altamente corrosivo, lo que requiere un manejo y almacenamiento cuidadosos en un área bien ventilada con el equipo de protección personal adecuado. Cloruro de metiloxalilo es soluble en disolventes orgánicos pero reacciona vigorosamente con agua, liberando ácido clorhídrico y formando oxalato de metilo. Se utiliza principalmente en síntesis orgánica, particularmente en la preparación de varios intermediarios químicos y en la producción de productos farmacéuticos y agroquímicos. Debido a su reactividad, presenta riesgos significativos para la salud, incluyendo irritación respiratoria y posibles quemaduras en la piel, lo que hace esencial seguir los protocolos de seguridad al trabajar con esta sustancia.
Fórmula:C3H3ClO3
InChI:InChI=1S/C3H3ClO3/c1-7-3(6)2(4)5/h1H3
Clave InChI:InChIKey=ZXUQEPZWVQIOJE-UHFFFAOYSA-N
SMILES:C(C(Cl)=O)(OC)=O
Sinónimos:- (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
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Encontrado 8 productos.
Methyl Chloroglyoxylate
CAS:Fórmula:C3H3ClO3Pureza:>98.0%(GC)(T)Forma y color:Colorless to Light yellow clear liquidPeso molecular: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>Fórmula:C3H3ClO3Pureza:97%Forma y color:Clear colorless, LiquidPeso molecular:122.50Methyl oxalyl chloride
CAS:Fórmula:C3H3ClO3Pureza:≥ 98.0%Forma y color:Colourless to light-yellow liquidPeso molecular:122.51METHYL (CHLOROCARBONYL)FORMATE
CAS:Fórmula:C3H3ClO3Pureza:97.0%Forma y color:LiquidPeso molecular:122.5Methyl Chlorooxoacetate
CAS:Producto controlado<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>Fórmula:C3H3ClO3Forma y color:NeatPeso molecular: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>Fórmula:C3H3ClO3Pureza:Min. 95%Forma y color:Clear LiquidPeso molecular:122.51 g/mol







