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CAS 20898-86-6

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2-(Chloromethyl)-5-nitrothiophene

Description:
2-(Chloromethyl)-5-nitrothiophene is a chemical compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a chloromethyl group (-CH2Cl) at the second position and a nitro group (-NO2) at the fifth position of the thiophene ring contributes to its reactivity and potential applications in organic synthesis and materials science. This compound typically exhibits a yellow to brown color and is soluble in organic solvents. Its structure allows for electrophilic substitution reactions, making it useful in the synthesis of various derivatives. The nitro group is a strong electron-withdrawing group, which can influence the compound's electronic properties and reactivity. Additionally, the chloromethyl group can serve as a versatile functional handle for further chemical modifications. Due to these characteristics, 2-(Chloromethyl)-5-nitrothiophene may find applications in pharmaceuticals, agrochemicals, and as an intermediate in the synthesis of more complex organic molecules. Safety precautions should be observed when handling this compound, as it may pose health risks.
Formula:C5H4ClNO2S
InChI:InChI=1S/C5H4ClNO2S/c6-3-4-1-2-5(10-4)7(8)9/h1-2H,3H2
InChI key:InChIKey=KHXIFJKSANMLQD-UHFFFAOYSA-N
SMILES:N(=O)(=O)C=1SC(CCl)=CC1
Synonyms:
  • 2-(Chloromethyl)-5-nitrothiophene
  • Thiophene, 2-(chloromethyl)-5-nitro-
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