Product Name:methyl 3-amino-5-(4-phenylphenyl)thiophene-2-carboxylate

IUPAC Name:methyl 3-amino-5-{[1,1'-biphenyl]-4-yl}thiophene-2-carboxylate

CAS:91076-97-0
Molecular Formula:C18H15NO2S
Purity:95%+
Catalog Number:CM671548
Molecular Weight:309.38

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Product Details

CAS NO:91076-97-0
Molecular Formula:C18H15NO2S
Melting Point:-
Smiles Code:COC(=O)C1=C(N)C=C(S1)C1=CC=C(C=C1)C1=CC=CC=C1
Density:
Catalog Number:CM671548
Molecular Weight:309.38
Boiling Point:
MDL No:MFCD04116405
Storage:

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.

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Product Other Information

Product Overview Methyl 3-amino-5-(4-phenylphenyl)thiophene-2-carboxylate is a chemical compound that has gained attention in the field of scientific research due to its potential applications in various fields. This compound is a thiophene derivative that has shown promising results in the field of medicinal chemistry, organic synthesis, and material science.
Synthesis Method One of the most commonly used methods is the reaction between 2-acetylthiophene and 4-phenylbenzaldehyde in the presence of ammonium acetate and methanol. The reaction yields the desired product with a high yield and purity.
Chemical Properties Methyl 3-amino-5-(4-phenylphenyl)thiophene-2-carboxylate in lab experiments is high yield and purity. One of the limitations of using this compound is its potential toxicity.
Synthesis and Application In the field of medicinal chemistry, this compound has shown promising results as an anticancer agent. Studies have shown that this compound can induce apoptosis in cancer cells and inhibit their proliferation. In the field of organic synthesis, Methyl 3-amino-5-(4-phenylphenyl)thiophene-2-carboxylate has been used as a building block for the synthesis of various complex molecules. This compound has also been used as a key intermediate in the synthesis of other thiophene derivatives. In the field of material science, Methyl 3-amino-5-(4-phenylphenyl)thiophene-2-carboxylate has been used as a dopant in the fabrication of organic light-emitting diodes (OLEDs). This compound has been shown to improve the efficiency and stability of OLEDs.
Future Directions One of the future directions is the development of new anticancer agents based on this compound. This compound has shown promising results as an anticancer agent, and further research may lead to the development of more effective and less toxic anticancer agents. Another future direction is the synthesis of new thiophene derivatives based on this compound. This compound has been used as a building block for the synthesis of various complex molecules, and further research may lead to the development of new thiophene derivatives with unique properties. Lastly, further research may be conducted on the potential applications of this compound in the field of material science. This compound has been used as a dopant in the fabrication of OLEDs, and further research may lead to the development of new materials with improved efficiency and stability.