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Isotiocianato de 3-(trifluorometil)fenilo, 98 %, Thermo Scientific Chemicals

Thermo Scientific Chemicals

Isotiocianato de 3-(trifluorometil)fenilo, 98 %, Thermo Scientific Chemicals

Name: Isotiocianato de 3-(trifluorometil)fenilo, 98 %, Thermo Scientific Chemicals
SKU: L11646.03
Price: 25.70 EUR

CAS: 1840-19-3 | C8H4F3NS | 203.182 g/mol

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Cantidad:

1 g

5 g

25 g

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Número de catálogo L11646.03

también denominado L11646-03

Precio (EUR)

25,70

Each

Cantidad:

1 g

Pedido a granel o personalizado

Precio (EUR)

25,70

Each

Identificadores químicos

CAS1840-19-3

IUPAC Name1-isothiocyanato-3-(trifluoromethyl)benzene

Molecular FormulaC8H4F3NS

InChI KeyGFEPANUKFYVALF-UHFFFAOYSA-N

SMILESFC(F)(F)C1=CC=CC(=C1)N=C=S

Especificaciones Specification Sheet

Hoja de especificaciones

CommentSpecification differs for U.S. and non-U.S. material where indicated

Identification (FTIR)Conforms (non-U.S. specification)

Refractive Index1.5530-1.5570 @ 20°C (non-U.S. specification)

Appearance (Color)Clear colorless to yellow

FormLiquid

Used as pharamaceutical intermediate.

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
Se utiliza como intermedio faramaceútico.

Solubilidad
Se hidroliza en agua.

Notas
Mantener el recipiente bien sellado. Almacenar en un lugar fresco y seco y en recipientes bien sellados. Incompatible con los agentes oxidantes. Es sensible a la humedad.

RUO – Research Use Only

General References:

Ha-Young Kim.; Se Hun Kwak.; Gee-Hyung Lee.; Young-Dae Gong. Copper-catalyzed synthesis of 3-substituted-5-amino-1,2,4-thiadiazoles via intramolecular N-S bond formation. Tetrahedron. 2014, 70 (45), 8737-8743.
Sara Van Poecke.; Hélène Munier-Lehmann.; Olivier Helynck.; Matheus Froeyend.; Serge Van Calenbergh. Synthesis and inhibitory activity of thymidine analogues targeting Mycobacterium tuberculosis thymidine monophosphate kinase. Bioorganic & Medicinal Chemistry. 2011, 19 (24), 7603-7611.