167482-90-8

Basic information

• Product Name: 5-(3,4,5-trimethoxyphenyl)dipyrromethane
• Synonyms: 5-(3,4,5-trimethoxyphenyl)dipyrromethane
• CAS NO: 167482-90-8
• Molecular Weight: 312.368
• Mol File: 167482-90-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 5-(3,4,5-trimethoxyphenyl)dipyrromethane(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(3,4,5-trimethoxyphenyl)dipyrromethane(167482-90-8)
• EPA Substance Registry System: 5-(3,4,5-trimethoxyphenyl)dipyrromethane(167482-90-8)

Safety Data

• Hazardous Substances Data: 167482-90-8(Hazardous Substances Data)

Upstream product

• 109-97-7 pyrrole 
• 253453-32-6 2-(3,4,5-trimethoxy)phenyltetrahydro-(2H)-1,3-oxazine 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 

Downstream Products

• 1456785-02-6 bis(5-(3,4,5-trimethoxyphenyl)dipyrrinato)iron(II) 
• 1456781-38-6 5-(3,4,5-trimethoxyphenyl)dipyrromethene 
• 360076-35-3 C₆₀H₄₄N₄O₈ 
• 158432-38-3 1,9-dicyano-5-(3',4',5'-trimethoxyphenyl)dipyrromethane 

Relevant articles and documents

Synthesis of 5,15-diarylporphyrins via orthoesters condensation with aryldipyrromethanes

General access to 5,15-diarylporphyrins in two steps is described. Generalization of this approach to tetra-substituted porphyrins allows the reproducible preparation of compounds, in some cases with high yields for porphyrins, which can be used in photodynamic therapy (PDT) in cancer today.

Unique versatility of Amberlyst 15. An acid and solvent-free paradigm towards synthesis of bis(heterocyclyl)methane derivatives

Bis(heterocyclyl)methanes, key intermediates for a variety of chemical, biochemical and material science relevant targets, have been obtained in a synthetically useful manner using Amberlyst 15 ion-exchange resin. This method promises versatility, cost-ef

Responsive and mitochondria-specific ruthenium(ii) complex for dual in vitro applications: Two-photon (near-infrared) induced imaging and regioselective cell killing

A mitochondria-permeable ruthenium(ii) complex has been designed as a responsive probe which may be used to sensitize the formation of singlet oxygen (ΦΔ = 0.93) and cause local damage in cellulo when exposed to UV and near-infrared laser excit