Thiophene-2-carboxaldehyde, 98+%, Thermo Scientific Chemicals
Thiophene-2-carboxaldehyde, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Thiophene-2-carboxaldehyde, 98+%, Thermo Scientific Chemicals

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Catalog number A14344.0B
also known as A14344-0B
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417.00
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Quantity:
1000 g
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Price (USD)/ Each
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Thiophene-2-carboxaldehyde, 98+%, Thermo Scientific Chemicals
Catalog numberA14344.0B
Price (USD)/ Each
417.00
-
Add to cart
Chemical Identifiers
CAS98-03-3
IUPAC Namethiophene-2-carbaldehyde
Molecular FormulaC5H4OS
InChI KeyCNUDBTRUORMMPA-UHFFFAOYSA-N
SMILESO=CC1=CC=CS1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow to brown
FormLiquid
Free acid (titration)<1.0%
Assay (GC)≥98.0%
Identification (FTIR)Conforms
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Thiophene-2-carboxaldehyde is used in the preparation of beta-aryl-beta-amino acids and urea derivatives. It acts as an arylation reagent. Further, it is used in the synthesis of unsaturated ketones, which serve as antiviral and cytotoxic agents. In addition to this, it is used as an intermediate to manufacture pharmaceuticals and aromatic compounds.

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
Thiophene-2-carboxaldehyde is used in the preparation of beta-aryl-beta-amino acids and urea derivatives. It acts as an arylation reagent. Further, it is used in the synthesis of unsaturated ketones, which serve as antiviral and cytotoxic agents. In addition to this, it is used as an intermediate to manufacture pharmaceuticals and aromatic compounds.

Solubility
Miscible with chloroform, alcohol, ether, dimethylsulfoxide, ethyl acetate and most organic solvents. Immiscible with water.

Notes
Store in a cool place. Incompatible with strong bases, strong oxidizing agents and strong reducing agents.
RUO – Research Use Only

General References:

  1. Sánchez, C. O.; Schott, E.; Zárate, X.; MacLeod-Carey, D.; Sobarzo, P.; Gatica, N. Effect of triphenylamine as electron-donor evenly spaced in 2, 4, 6 and 8 thiophene units of the main chain: synthesis and properties. Polym. Bull. 2015, 72 (4), 897-913.
  2. Sánchez, C. O.; Sobarzo, P.; Gatica, N. Electronic and structural properties of polymers based on phenylene vinylene and thiophene units. Control of the gap by gradual increases of thiophene moieties. New J. Chem. 2015, 39 (10), 7979-7987.