Metil metoxiacetato, 99 %, Thermo Scientific Chemicals

CAS: 6290-49-9 | C4H8O3 | 104.11 g/mol

Número de catálogo	Cantidad
B22528.36 también denominado B22528-36	500 g

Número de catálogo B22528.36

también denominado B22528-36

Precio (USD)

Cantidad:

500 g

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Identificadores químicos

CAS6290-49-9

IUPAC Namemethyl 2-methoxyacetate

Molecular FormulaC4H8O3

InChI KeyQRMHDGWGLNLHMN-UHFFFAOYSA-N

SMILESCOCC(=O)OC

Especificaciones Specification Sheet

Assay (GC)≥98.5%

Identification (FTIR)Conforms

Refractive Index1.3955-1.3985 @ 20?C

Appearance (Color)Clear colorless

FormLiquid

Methyl methoxyacetate is used in the preparation of 4-hydroxy-2-mercapto-5-methoxypyrimidine (II).

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 Scientific Chemicals.

Aplicaciones
El metoxiacetato de metilo se utiliza en la preparación de 4-hidroxi-2-mercapto-5-metoxipirimidina (II).

Solubilidad
Soluble en agua.

Notas
Mantener el recipiente herméticamente cerrado. Almacénese lejos de los agentes oxidantes.

RUO – Research Use Only

General References:

Qiuhua Li.; Chuanhui Huang.; Tongwen Xu. Bipolar membrane electrodialysis in an organic medium: Production of methyl methoxyacetate. Journal of Membrane Science. 2009, 339, (1-2), 28-32.
Qiuhua Li.; Chuanhui Huang.; Tongwen Xu. Alcohol splitting for the production of methyl methoxyacetate: Integration of ion-exchange with bipolar membrane electrodialysis. Journal of Membrane Science. 2011, 367, (1-2), 314-318.
The ɑ-lithio-derivative adds to ketones in the normal manner. Elimination of water provides a useful synthesis of ɑ-methoxyacrylates: Tetrahedron Lett., 2825 (1977).