CAS 4075-59-6
:2-Thiopheneglyoxylic acid
Description:
2-Thiopheneglyoxylic acid, with the CAS number 4075-59-6, is an organic compound characterized by the presence of both a thiophene ring and a glyoxylic acid functional group. This compound typically appears as a white to light yellow crystalline solid. It is known for its acidic properties due to the carboxylic acid group, which can participate in various chemical reactions, including esterification and amidation. The thiophene moiety contributes to its aromatic character and can influence its reactivity and solubility in organic solvents. 2-Thiopheneglyoxylic acid is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to serve as a building block for more complex molecules. Additionally, its unique structure allows for potential applications in materials science and as a ligand in coordination chemistry. As with many organic acids, it is important to handle this compound with care, observing appropriate safety protocols to mitigate any risks associated with its use.
Formula:C6H4O3S
InChI:InChI=1S/C6H4O3S/c7-5(6(8)9)4-2-1-3-10-4/h1-3H,(H,8,9)
InChI key:InChIKey=GIWRVUADKUVEGU-UHFFFAOYSA-N
SMILES:C(C(O)=O)(=O)C1=CC=CS1
Synonyms:- (2-Thienyl)oxoacetic acid
- 2-(2-Thienyl)-2-oxoacetic acid
- 2-Oxo-2-(2-thienyl)acetic acid
- 2-Oxo-2-(thiophen-2-yl)acetic acid
- 2-Thienylglyoxalic acid
- 2-Thienylglyoxylic Acid
- 2-Thiopenylglyoxylic Acid
- 2-Thiopheneacetic acid, α-oxo-
- 2-Thiopheneglyoxylic acid
- Oxo(Thiophen-2-Yl)Acetate
- Oxo(Thiophen-2-Yl)Acetic Acid
- Oxo(thien-2-yl)acetic acid
- α-Oxo-2-thiopheneacetic acid
- See more synonyms
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Found 3 products.
2-Oxo-2-(thiophen-2-yl)acetic acid
CAS:Formula:C6H4O3SPurity:96%Color and Shape:SolidMolecular weight:156.1592Oxo(thien-2-yl)acetic acid
CAS:<p>Oxo(thien-2-yl)acetic acid</p>Formula:C6H4O3SPurity:96%Color and Shape: light yellow solidMolecular weight:156.16g/molThiophene-2-glyoxylic acid
CAS:<p>Thiophene-2-glyoxylic acid is a reactive metabolite of thiophene that is formed from the environmental degradation of this compound. Thiophene-2-glyoxylic acid reacts with halides to form an electrophilic intermediate. This intermediate can react with a variety of nucleophiles, including the drug metabolites, leading to the formation of new compounds. Thiophene-2-glyoxylic acid has been shown to enhance the fluorescence properties of some organic compounds. It also has been shown to inhibit the metabolism of some drugs that are conjugated with acids and can be detected in plasma by mass spectrometry.</p>Formula:C6H4O3SPurity:Min. 95%Color and Shape:PowderMolecular weight:156.16 g/mol


