367254-81-7

Basic information

• Product Name: ethyl 5-[(5-ethoxycarbonyl-3-methyl-4-phenyl-1H-pyrrol-2-yl)phenylmethyl]-4-methyl-3-phenyl-1H-pyrrole-2-carboxylate
• Synonyms: ethyl 5-[(5-ethoxycarbonyl-3-methyl-4-phenyl-1H-pyrrol-2-yl)phenylmethyl]-4-methyl-3-phenyl-1H-pyrrole-2-carboxylate
• CAS NO: 367254-81-7
• Molecular Weight: 546.666
• Mol File: 367254-81-7.mol

Chemical Properties

• CAS DataBase Reference: ethyl 5-[(5-ethoxycarbonyl-3-methyl-4-phenyl-1H-pyrrol-2-yl)phenylmethyl]-4-methyl-3-phenyl-1H-pyrrole-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 5-[(5-ethoxycarbonyl-3-methyl-4-phenyl-1H-pyrrol-2-yl)phenylmethyl]-4-methyl-3-phenyl-1H-pyrrole-2-carboxylate(367254-81-7)
• EPA Substance Registry System: ethyl 5-[(5-ethoxycarbonyl-3-methyl-4-phenyl-1H-pyrrol-2-yl)phenylmethyl]-4-methyl-3-phenyl-1H-pyrrole-2-carboxylate(367254-81-7)

Safety Data

• Hazardous Substances Data: 367254-81-7(Hazardous Substances Data)

Upstream product

• 66618-80-2 1-phenyl-2-nitro-1-propanol acetate 
• 100-52-7 benzaldehyde 
• 26251-08-1 2-nitro-1-phenylpropan-1-ol 
• 705-60-2 1-phenyl-2-nitroprop-1-ene 
• 2999-46-4 Ethyl isocyanoacetate 
• 124901-12-8 ethyl 4-methyl-3-phenyl-1H-pyrrole-2-carboxylate 

Downstream Products

• 367254-33-9 5-[(5-carboxy-3-methyl-4-phenyl-1H-pyrrol-2-yl)phenylmethyl]-4-methyl-3-phenyl-1H-pyrrole-2-carboxylic acid 
• 936261-69-7 C₄₃H₃₈N₆O₂ 

Relevant articles and documents

Preparation of diverse BODIPY diesters

The synthesis and properties of a variety of substituted BODIPY diesters is presented. We find that certain substitution patterns afford appreciable yields of the target compounds and that electronic effects result in predicable differential fluorescent behavior. Challenges to further water solubilize these dyes and/or provide new points of attachment for biological tagging remain, these strategies are discussed.

Synthesis of new polydentate tweezers ligands of amido-amine type

A series of new tweezers amido-amine ligands containing pyrrole, bipyrrole, and dipyrrolylmethane fragments were synthesized by reaction of 2-thioxothiazolidin-3-yl derivatives of α-pyrrolecarboxylic acids {5-[1-(5-carboxy-3-methyl-4-phenyl-1H-pyrrol-2-yl