2-Thiopheneacetic acid, 98%

Name: 2-Thiopheneacetic acid, 98%
SKU: A10394.36

CAS: 1918-77-0 | C6H6O2S | 142.172 g/mol

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Catalog number A10394.36

also known as A10394-36

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Chemical Identifiers

CAS1918-77-0

IUPAC Name2-(thiophen-2-yl)acetic acid

Molecular FormulaC6H6O2S

InChI KeySMJRBWINMFUUDS-UHFFFAOYSA-N

SMILESOC(=O)CC1=CC=CS1

Specifications

Specification Sheet

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

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.

Applications
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.

Solubility
Soluble in water, ethanol, ether and carbon tetrachloride.

Notes
Incompatible with strong oxidizing agents and strong bases.

RUO – Research Use Only

General References:

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.
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.