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Cloruro de acetoxiacetilo, 97 %, Thermo Scientific Chemicals

Thermo Scientific Chemicals

Cloruro de acetoxiacetilo, 97 %, Thermo Scientific Chemicals

Name: Cloruro de acetoxiacetilo, 97 %, Thermo Scientific Chemicals
SKU: H25797.14
Price: 110.00 EUR

CAS: 13831-31-7 | C4H5ClO3 | 136.531 g/mol

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Cantidad:

5 g

25 g

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Número de catálogo H25797.14

también denominado H25797-14

Precio (EUR)

110,00

Each

Cantidad:

25 g

Pedido a granel o personalizado

Precio (EUR)

110,00

Each

Identificadores químicos

CAS13831-31-7

IUPAC Name2-chloro-2-oxoethyl acetate

Molecular FormulaC4H5ClO3

InChI KeyHZDNNJABYXNPPV-UHFFFAOYSA-N

SMILESCC(=O)OCC(Cl)=O

Especificaciones Specification Sheet

Hoja de especificaciones

Refractive Index1.4245-1.4295 @ 20°C (non-U.S. sourced material)

Appearance (Color)Clear colorless to pale yellow

FormLiquid

Assay (GC)≥96.0%

CommentMaterial Sourced in the U.S. and in other countries

Acetoxyacetyl chloride was used in synthesis of stabilized axial and equatorial conformers of spiro-β-lactams and glycolylhydroxamic acids.

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 cloruro de acetoxiacetilo se utilizó en la síntesis de confórmeros axiales y ecuatoriales estabilizados de espiroβlactamas y ácidos glicolilhidroxámicos.

Solubilidad
Reacciona violentamente con el agua.

Notas
Sensible a la humedad. Almacenar alejado de agentes oxidantes, bases y agua/humedad.

RUO – Research Use Only

General References:

Hiromune Ando;, Yusuke Koike; Hideharu Ishida; Makoto Kiso. Extending the possibility of an N-Troc-protected sialic acid donor toward variant sialo-glycoside synthesis. Tetrahedron Letters. 2003, 44 (36), 6883-6886.
OM Walsh; MJ Meegan; RM Prendergast; T Al Nakib. Synthesis of 3-acetoxyazetidin-2-ones and 3-hydroxyazetidin-2-ones with antifungal and antibacterial activity. European Journal of Medicinal Chemistry. 1996, 31 (12), 989-1000.