CAS 88770-22-3
:3-Thiophenecarboxylic acid, 5-nitro-, methyl ester
Description:
3-Thiophenecarboxylic acid, 5-nitro-, methyl ester is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group that is esterified with a methyl group, as well as a nitro group positioned at the 5th carbon of the thiophene ring. The presence of the nitro group introduces electron-withdrawing properties, which can influence the compound's reactivity and polarity. Typically, compounds like this exhibit moderate solubility in organic solvents and may have limited solubility in water due to the hydrophobic nature of the thiophene ring. The compound may be of interest in various fields, including pharmaceuticals and materials science, due to its potential biological activity and utility in synthetic applications. As with many organic compounds, safety precautions should be taken when handling, as it may pose health risks or environmental hazards.
Formula:C6H5NO4S
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
3-Thiophenecarboxylic acid, 5-nitro-, methyl ester
CAS:Formula:C6H5NO4SPurity:%Color and Shape:SolidMolecular weight:187.1732Ref: 10-F665627
1g539.00€5g1,483.00€10g2,222.00€2.5g1,111.00€50mg137.00€100mg177.00€250mg252.00€500mg435.00€Methyl 5-nitrothiophene-3-carboxylate
CAS:Methyl 5-nitrothiophene-3-carboxylate is a dienophile that reacts with electron-rich diene compounds to form substituted benzothiophenes by the Diels-Alder reaction. The electron acceptor in this reaction is the diene, and the electron donor is methyl 5-nitrothiophene-3-carboxylate. The selectivity of this reaction can be controlled by altering the substitution pattern on the diene. The cycloaddition product is a monocyclic system containing four fused rings and one unsaturated bond. This product is also known as an indanone.Formula:C6H5NO4SPurity:Min. 95%Molecular weight:187.18 g/mol
