| Weight | 128.152 g/mol |
|---|---|
| Formula | C5H4O2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
THIOPHENE-2-CARBOXYLIC ACID (527-72-0)
thiophene-2-carboxylate, 2-(14)C-labeled · thiophene-2-carboxylate · sodium thiophenecarboxylate
Score:
#1939 in Physics
,
#6077 in Chemistry
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- Direct synthesis of benzo[b]thiophene-2-carboxylate esters involving nitro displacement (Journal of Organic Chemistry, 1972)
- A highly sensitive and selective fluorescent sensor for Al3+ ions based on thiophene-2-carboxylic acid hydrazide Schiff base (RSC Advances, 2013)
- Nonbasic, Room Temperature, Palladium-Catalyzed Coupling of Aryl and Alkenyl Iodides with Boronic Acids Mediated by Copper(I) Thiophene-2-carboxylate (CuTC) (Organic Letters, 2001)
- Calix[2]bipyrrole[2]furan and calix[2]bipyrrole[2]thiophene: New pyrrolic receptors exhibiting a preference for carboxylate anions (Journal of the American Chemical Society, 2003)
- Structural chemistry of organotin carboxylates. XII, Synthesis and characterization of diorganotin(IV) carboxylates containing 2-thiophene- or 2-furan-carboxylic acid. Crystal structure of [ET2Sn(O2CC4H3S)2] (Journal of Organometallic Chemistry, 1991)
- Synthesis, characterization and crystal structures of the organotin(IV) compounds with the Schiff base ligands of pyruvic acid thiophene-2-carboxylic hydrazone and salicylaldehyde thiophene-2-carboxylic hydrazone (Inorganica Chimica Acta, 2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - thiophene-2-carboxylate, 2-(14)C-labeled
- thiophene-2-carboxylate
- sodium thiophenecarboxylate
- thiophene-2-carboxylate, sodium salt
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SMILESC1=CSC(=C1)C(=O)O
-
InChIKeyQERYCTSHXKAMIS-UHFFFAOYSA-N
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THIOPHENE-2-CARBOXYLIC ACID
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