
CAS 166887-84-9
:2-(bromomethyl)-5-nitrothiophene
Description:
2-(Bromomethyl)-5-nitrothiophene is an organic compound characterized by its thiophene ring, which is a five-membered heterocyclic structure containing sulfur. The presence of a bromomethyl group at the second position and a nitro group at the fifth position contributes to its reactivity and potential applications in organic synthesis and materials science. This compound typically exhibits a yellow to brown coloration and is soluble in organic solvents, reflecting its non-polar characteristics. The bromomethyl group can serve as a versatile electrophile in various chemical reactions, while the nitro group can influence the electronic properties of the molecule, making it a candidate for further functionalization. Additionally, the compound's structure suggests potential applications in the development of pharmaceuticals, agrochemicals, or as intermediates in the synthesis of more complex organic molecules. Safety precautions should be taken when handling this compound, as both brominated and nitro compounds can pose health risks.
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Found 4 products.
Thiophene, 2-(bromomethyl)-5-nitro-
CAS:Formula:C5H4BrNO2SPurity:97%Color and Shape:LiquidMolecular weight:222.05982-(Bromomethyl)-5-nitrothiophene
CAS:2-(Bromomethyl)-5-nitrothiophenePurity:97%Molecular weight:222.06g/mol2-(BROMOMETHYL)-5-NITROTHIOPHENE
CAS:Formula:C5H4BrNO2SPurity:97%Color and Shape:LiquidMolecular weight:222.062-(Bromomethyl)-5-nitrothiophene
CAS:<p>2-(Bromomethyl)-5-nitrothiophene is a compound that belongs to the class of organic compounds known as thiophenes. It can be used as an optoelectronic material, and has been shown to have a transition from a triplet state to a singlet state at room temperature. It is also an acceptor in tetrads, which are molecules that have four electron pairs. The triplet state of 2-(bromomethyl)-5-nitrothiophene is able to emit light in the visible spectrum when exposed to UV light.</p>Formula:C5H4BrNO2SPurity:Min. 95%Molecular weight:222.06 g/mol




