Ácido 2-tiofenoacético, 98 %, Thermo Scientific Chemicals
Ácido 2-tiofenoacético, 98 %, Thermo Scientific Chemicals
Ácido 2-tiofenoacético, 98 %, Thermo Scientific Chemicals
Ácido 2-tiofenoacético, 98 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ácido 2-tiofenoacético, 98 %, Thermo Scientific Chemicals

CAS: 1918-77-0 | C6H6O2S | 142.172 g/mol
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Cantidad:
25 g
100 g
500 g
Número de catálogo A10394.36
también denominado A10394-36
Precio (USD)
-
Cantidad:
500 g
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Identificadores químicos
CAS1918-77-0
IUPAC Name2-(thiophen-2-yl)acetic acid
Molecular FormulaC6H6O2S
InChI KeySMJRBWINMFUUDS-UHFFFAOYSA-N
SMILESOC(=O)CC1=CC=CS1
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EspecificacionesSpecification SheetHoja de especificaciones
CommentMaterial sourced in the U.S. and in other countries
Melting Point (clear melt)61-66°C
Assay (HPLC)≥97.5%
Identification (FTIR)Conforms (non-U.S. sourced material)
Appearance (Color)White to grey or brown
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2-Thiopheneacetic acid is used in the preparation of rosette-like nanoscale gold materials. Further, it is used as a pharmaceutical intermediate for cefaloridine and cefalotin sodium.

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 ácido 2-tiofeneacético se utiliza en la preparación de materiales de oro a nanoescala como la roseta. Además, se usa como intermedio farmacéutico para la cefaloridina y la cefalotina sódica.

Solubilidad
Soluble en agua, etanol, éter y tetracloruro de carbono.

Notas
Incompatible con agentes oxidantes fuertes y bases fuertes.
RUO – Research Use Only

General References:

  1. Bae, S. E.; Kim, K. J.; Hwang, Y. K.; Huh, S. Simple preparation of Pd-NP/polythiophene nanospheres for heterogeneous catalysis. J. Colloid Interface Sci. 2015, 456, 93-99.
  2. Chen, X.; Chen, T.; Ji, F.; Zhou, Y.; Yin, S. F. Iron-catalyzed aerobic oxidative functionalization of sp3 C-H bonds: a versatile strategy for the construction of N-heterocycles. Catal. Sci. Technol. 2015, 5 (4), 2197-2202.