CAS 10472-24-9
:Metil 2-oxociclopentanocarboxilato
Descripción:
Metil 2-oxociclopentanocarboxilato, con el número CAS 10472-24-9, es un compuesto orgánico caracterizado por su estructura cíclica y grupos funcionales. Presenta un anillo de ciclopentano con un grupo cetona (2-oxo) y un grupo carboxilato (éster), que contribuyen a su reactividad y aplicaciones potenciales en síntesis orgánica. Este compuesto es típicamente un líquido incoloro a amarillo pálido, que exhibe un olor agradable. Es soluble en disolventes orgánicos, lo que lo hace útil en varias reacciones y procesos químicos. La presencia del grupo funcional éster permite la participación en reacciones de sustitución acilo nucleofílica, mientras que el grupo cetona puede sufrir transformaciones adicionales como reducción o condensación. Metil 2-oxociclopentanocarboxilato puede ser utilizado en la síntesis de moléculas más complejas, incluidos productos farmacéuticos y agroquímicos. Al igual que muchos compuestos orgánicos, debe manejarse con cuidado, observando los protocolos de seguridad apropiados para mitigar cualquier riesgo asociado con su uso.
Fórmula:C7H10O3
InChI:InChI=1S/C7H10O3/c1-10-7(9)5-3-2-4-6(5)8/h5H,2-4H2,1H3
Clave InChI:InChIKey=PZBBESSUKAHBHD-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1C(=O)CCC1
Sinónimos:- 2-(Methoxycarbonyl)cyclopentanone
- 2-Carbomethoxycyclopentanone
- 2-Cyclopentanonecarboxylic acid methyl ester
- 2-Methoxy Carbonyl Cyclopentanone
- 2-Oxocyclopentanecarboxylic acid methyl ester
- Cyclopentanecarboxylic acid, 2-oxo-, methyl ester
- Cyclopentanone-2-carboxylic acid methyl ester
- Cyclopentenone-2-carboxylic acid methyl ester
- Ethyl (4-Methylphenyl)Acetate
- Methyl 2-Oxocyclopentane-1-Carboxylate
- Methyl 2-cyclopentanone carboxylate
- Methyl 2-cyclopentanone-1-carboxylate
- Methyl 2-oxo-1-cyclopentanecarboxylate
- Methyl 2-oxocyclopentacarboxylate
- Methyl 2-oxocyclopentan-1-carboxylate
- Methyl 2-oxocyclopentanecarboxylate
- Methyl cyclopentanone-2-carboxylate
- Methyl-2-cyclopentnonecrboxylte
- Methyl-2-oxocyclopentane carboxylate
- methyl (1R)-2-oxocyclopentanecarboxylate
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Encontrado 9 productos.
Methyl 2-Oxocyclopentanecarboxylate
CAS:Fórmula:C7H10O3Pureza:>97.0%(GC)Forma y color:Colorless to Light yellow clear liquidPeso molecular:142.15Methyl 2-cyclopentanonecarboxylate
CAS:Fórmula:C7H10O3Pureza:95%Forma y color:Liquid, ClearPeso molecular:142.154Methyl 2-oxocyclopentanecarboxylate, 97%
CAS:<p>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 Sci</p>Fórmula:C7H10O3Pureza:97%Forma y color:Clear colorless to pale pink, LiquidPeso molecular:142.15Methyl 2-Cyclopentanonecarboxylate
CAS:Fórmula:C7H10O3Pureza:95%Forma y color:LiquidPeso molecular:142.1525Ref: IN-DA003RNQ
5gA consultar10gA consultar25g20,00€5kg187,00€100g25,00€250g34,00€25kgA consultar500g53,00€Methyl 2-oxocyclopentane-1-carboxylate
CAS:<p>Methyl 2-oxocyclopentane-1-carboxylate</p>Fórmula:C7H10O3Pureza:99%Forma y color: clear. colourless liquidPeso molecular:142.15249g/molMethyl-2-oxycyclopentanecarboxylate
CAS:<p>Methyl-2-oxycyclopentanecarboxylate is an enolate that is used as a sealant. It reacts with the hydroxy group of polymers such as polyvinyl alcohol, polyvinyl acetate, polyvinyl chloride, and polyurethane to form crosslinked structures. Methyl-2-oxycyclopentanecarboxylate is also used in asymmetric syntheses to form chiral products. The monomers are methylated by the addition of methanol or dimethyl hexanedioate, and then reacted with squaramide (1,4-dioxaspiro[4.5]decane) to form a symmetrical dimer of chiral cyclopentanone. This reaction can be catalyzed by hydrogen bonding between the methyl group and the carbonyl group in squaramide.</p>Fórmula:C7H10O3Pureza:Min. 95%Forma y color:Clear LiquidPeso molecular:142.15 g/molMethyl 2-Cyclopentanonecarboxylate
CAS:Producto controlado<p>Applications Methyl 2-Cyclopentanonecarboxylate is used in the synthesis of functionalized ketones.<br>References Mashima, K. et al.: J. Org. Chem., 59, 3064 (1994); Hamashima, Y. et al.: J. Am. Chem. Soc., 124, 11240 (2002);<br></p>Fórmula:C7H10O3Forma y color:NeatPeso molecular:142.15








