Thiophene, 2-chloro-5-nitro- (CAS 13195-49-8) is a heterocyclic organic compound characterized by a five-membered aromatic ring containing sulfur. The presence of a chlorine atom at the second position and a nitro group at the fifth position of the thiophene ring contributes to its unique chemical properties. This compound typically exhibits a yellow to brown color and is soluble in organic solvents. It is known for its reactivity, particularly in electrophilic substitution reactions due to the electron-withdrawing effects of the nitro group and the halogen. The compound may also participate in nucleophilic reactions, making it valuable in synthetic organic chemistry. Additionally, thiophene derivatives are often studied for their potential applications in materials science, pharmaceuticals, and agrochemicals. Safety precautions should be observed when handling this compound, as it may pose health risks, including toxicity and environmental hazards. Overall, thiophene, 2-chloro-5-nitro- is an important compound in the field of organic synthesis and materials development.

Thiophene, 2-chloro-5-nitro-

13195-49-8: Thiophene, 2-chloro-5-nitro- (CAS 13195-49-8) is a heterocyclic organic compound characterized by a five-membered aromatic ring containing sulfur. The presence of a chlorine atom at the second position and a nitro group at the fifth position of the thiophene ring contributes to its unique chemical properties. This compound typically exhibits a yellow to brown color and is soluble in organic solvents. It is known for its reactivity, particularly in electrophilic substitution reactions due to the electron-withdrawing effects of the nitro group and the halogen. The compound may also participate in nucleophilic reactions, making it valuable in synthetic organic chemistry. Additionally, thiophene derivatives are often studied for their potential applications in materials science, pharmaceuticals, and agrochemicals. Safety precautions should be observed when handling this compound, as it may pose health risks, including toxicity and environmental hazards. Overall, thiophene, 2-chloro-5-nitro- is an important compound in the field of organic synthesis and materials development.

<p>2-Chloro-5-nitrothiophene is a nucleophilic compound that reacts with acetonitrile, which is a nucleophile. The inhibitory concentration of 2-chloro-5-nitrothiophene has been shown to be lower than that of thiophenes in general, and the compound can be used as a tool for evaluating the biological activity of thiophenes. 2-Chloro-5-nitrothiophene has been shown to have good inhibitory effects on Escherichia coli and other organisms. This compound also induces a number of different reactions: heterocyclic ring formation, synthesis of acetonitrile, and biomolecule evaluation.</p>

CAS 13195-49-8

Thiophene, 2-chloro-5-nitro-

Thiophene, 2-chloro-5-nitro-

Ref: IN-DA000ZYB

2-chloro-5-nitrothiophene

Ref: 3D-NAA19549