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CAS 143468-96-6

:

1-Ethyl 2-(2-thienylmethyl)propanedioate

Description:
1-Ethyl 2-(2-thienylmethyl)propanedioate, identified by its CAS number 143468-96-6, is an organic compound characterized by its unique structure, which includes an ethyl group and a thienylmethyl substituent attached to a propanedioate backbone. This compound features two ester functional groups, contributing to its reactivity and potential applications in organic synthesis. The presence of the thienyl ring, a five-membered aromatic heterocycle containing sulfur, imparts distinct electronic properties and can influence the compound's solubility and interaction with other molecules. Typically, compounds of this nature may exhibit moderate to high polarity due to the ester groups, affecting their behavior in various solvents. Additionally, the thienyl moiety can enhance biological activity, making such compounds of interest in pharmaceutical research. Overall, 1-Ethyl 2-(2-thienylmethyl)propanedioate represents a versatile structure that may serve as a building block in the synthesis of more complex organic molecules.
Formula:C10H12O4S
InChI:InChI=1S/C10H12O4S/c1-2-14-10(13)8(9(11)12)6-7-4-3-5-15-7/h3-5,8H,2,6H2,1H3,(H,11,12)
InChI key:InChIKey=PMJNEQWWZRSFCE-UHFFFAOYSA-N
SMILES:C(C(C(OCC)=O)C(O)=O)C1=CC=CS1
Synonyms:
  • (2-Thienylmethyl)propanedioic acid monoethyl ester
  • 1-Ethyl 2-(2-thienylmethyl)propanedioate
  • 2-(Ethoxycarbonyl)-3-(thien-2-yl)propanoic acid
  • 2-Carbethoxy-3-(2-Thienyl) Propanoic acid
  • 3-Ethoxy-3-Oxo-2-(Thiophen-2-Ylmethyl)Propanoic Acid
  • Propanedioic acid, (2-thienylmethyl)-, monoethyl ester
  • Propanedioic acid, 2-(2-thienylmethyl)-, 1-ethyl ester
  • Ethyl 2-carboxy-3-(2-thienyl)propionate
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