CAS 1415562-73-0

Methyl 5-[(3-bromo-4-methyl-2-pyridinyl)[(1,1-dimethylethoxy)carbonyl]amino]-3′-(ethylsulfonyl)-4-methyl[1,1′-biphenyl]-3-carboxylate

Description:

Methyl 5-[(3-bromo-4-methyl-2-pyridinyl)[(1,1-dimethylethoxy)carbonyl]amino]-3′-(ethylsulfonyl)-4-methyl[1,1′-biphenyl]-3-carboxylate is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups such as a carboxylate, sulfonyl, and amine. The presence of a bromine atom and a pyridine ring contributes to its potential biological activity, making it of interest in medicinal chemistry. The compound features a biphenyl moiety, which can influence its electronic properties and interactions with biological targets. Additionally, the dimethylethoxycarbonyl group enhances its stability and solubility, which are crucial for its application in drug development. Its synthesis and characterization typically involve advanced organic chemistry techniques, and it may exhibit specific reactivity patterns due to the presence of electron-withdrawing and donating groups. Overall, this compound represents a significant example of the complexity found in modern organic synthesis, particularly in the context of pharmaceutical research.

Formula: C₂₈H₃₁BrN₂O₆S

InChI: InChI=1S/C28H31BrN2O6S/c1-8-38(34,35)21-11-9-10-19(14-21)20-15-22(26(32)36-7)18(3)23(16-20)31(27(33)37-28(4,5)6)25-24(29)17(2)12-13-30-25/h9-16H,8H2,1-7H3

InChI key: InChIKey=HXISPCSTQZMVTF-UHFFFAOYSA-N

SMILES: N(C(OC(C)(C)C)=O)(C1=CC(=CC(C(OC)=O)=C1C)C2=CC(S(CC)(=O)=O)=CC=C2)C3=C(Br)C(C)=CC=N3

Synonyms:

• [1,1′-Biphenyl]-3-carboxylic acid, 5-[(3-bromo-4-methyl-2-pyridinyl)[(1,1-dimethylethoxy)carbonyl]amino]-3′-(ethylsulfonyl)-4-methyl-, methyl ester
• Methyl 5-[(3-bromo-4-methyl-2-pyridinyl)[(1,1-dimethylethoxy)carbonyl]amino]-3′-(ethylsulfonyl)-4-methyl[1,1′-biphenyl]-3-carboxylate

Methyl 5-((3-bromo-4-methylpyridin-2-yl)(tert-butoxycarbonyl)amino)-3-(ethylsulfonyl)-4-methylbiphenyl-3-carboxylate

CAS: 1415562-73-0

Methyl 5-((3-bromo-4-methylpyridin-2-yl)(tert-butoxycarbonyl)amino)-3-(ethylsulfonyl)-4-methylbiphenyl-3-carboxylate is a peptide inhibitor that blocks the interaction of proteins with their targets. It has been shown to inhibit protein interactions and activate protein complexes. This product is an excellent research tool for studying ligand receptor interactions. Methyl 5-(3-(4-(5,6,7,8 tetrahydroquinazolin-2(1H)-yl)pyridin-2(1H)-yl)ethoxycarbonylamino)-3-(ethylsulfonyl)-4 methylbiphenyl 3 carboxylate has been shown to bind to ion channels and antibody sites on cells. The chemical name for this compound is: 5-[(3Bromo4methylpyr

Formula: C₂₈H₃₁BrN₂O₆S

Purity: Min. 95%

Molecular weight: 603.5 g/mol

Ref: 3D-QGC56273