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Bromoacetato de metilo, + 98 %, Thermo Scientific Chemicals

Thermo Scientific Chemicals

Bromoacetato de metilo, + 98 %, Thermo Scientific Chemicals

Name: Bromoacetato de metilo, + 98 %, Thermo Scientific Chemicals
SKU: A10605.0B
Price: 268.00 EUR

CAS: 96-32-2 | C3H5BrO2 | 152.975 g/mol

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Número de catálogo A10605.0B

también denominado A10605-0B

Precio (EUR)

268,00

Each

Cantidad:

1000 g

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Precio (EUR)

268,00

Each

Identificadores químicos

CAS96-32-2

IUPAC Namemethyl 2-bromoacetate

Molecular FormulaC3H5BrO2

InChI KeyYDCHPLOFQATIDS-UHFFFAOYSA-N

SMILESCOC(=O)CBr

Especificaciones Specification Sheet

Hoja de especificaciones

Refractive Index1.4565 - 1.4605 @20?C

FormLiquid

Appearance (Color)Clear colorless to pale yellow

Identification (FTIR)Conforms

Assay (GC)≥98.0%

Methyl bromoacetate is used in the synthesis of coumarins and cis-cyclopropanes. It reacts with the conjugate base of (methylmethoxycarbene)pentacarbonylchromium(0) to prepare alkylated carbene complexes. Further, it is used to make vitamins and pharmaceuticals.

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 bromoacetato de metilo se utiliza en la síntesis de cumarina y cis-ciclopropanos. Reacciona con la base conjugada de (metilmetoxicarbeno)pentacarbonilcromo(0) para preparar complejos de carbeno alquilados. Además, se utiliza para fabricar vitaminas y productos farmacéuticos.

Solubilidad
Miscible con metanol, éter y acetona. Ligeramente miscible con agua

Notas
Incompatibles con ácidos, bases, agentes oxidantes y agentes reductores.

RUO – Research Use Only

General References:

Dib, J.; Schlörer, N.; Schänzer, W.; Thevis, M. Studies on the collision-induced dissociation of adipoR agonists after electrospray ionization and their implementation in sports drug testing. J. Mass Spectrom. 2015, 50 (2), 407-417.
Hoashi, Y.; Takai, T.; Koike, T.; Uchikawa, O. Synthesis of a novel tricyclic 1, 6, 7, 8-tetrahydro-2H-cyclopenta [b] furo [3, 2-d] pyridine derivative, the 5-aza analog of ramelteon. Tetrahedron Lett. 2014, 55 (29), 4014-4016.