85857-14-3

Basic information

• Product Name: 5,10,15,20-tetrakis(p-chloromethylphenyl)porphyrin
• Synonyms: 5,10,15,20-tetrakis(p-chloromethylphenyl)porphyrin
• CAS NO: 85857-14-3
• Molecular Weight: 808.637
• Mol File: 85857-14-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5,10,15,20-tetrakis(p-chloromethylphenyl)porphyrin(CAS DataBase Reference)
• NIST Chemistry Reference: 5,10,15,20-tetrakis(p-chloromethylphenyl)porphyrin(85857-14-3)
• EPA Substance Registry System: 5,10,15,20-tetrakis(p-chloromethylphenyl)porphyrin(85857-14-3)

Safety Data

• Hazardous Substances Data: 85857-14-3(Hazardous Substances Data)

Upstream product

• 109-97-7 pyrrole 
• 73291-09-5 4-chloromethylbenzaldehyde 
• 22112-83-0 5,10,15,20-tetrakis(4-methoxycarbonylphenyl)porphyrin 
• 50-00-0 formaldehyd 
• 917-23-7 5,15,10,20-tetraphenylporphyrin 
• 1571-08-0 methyl 4-formylbenzoate 
• 182185-47-3 [4-(4-Methoxymethyl-[1,3]dioxolan-2-yl)-phenyl]-methanol 
• 14945-25-6 5,10,15,20-tetrakis-(4-hydroxymethylphenyl)porphyrin 
• 182185-45-1 4-(4-Methoxymethyl-[1,3]dioxolan-2-yl)-benzoic acid methyl ester 

Downstream Products

• 131026-18-1 meso tetrakis(4-(trimethylammonium)benzyl)porphyrin 

Relevant articles and documents

Phosphoniumyl cationic porphyrins Self-aggregation origin from π-π and cation-π interactions

The electrospectroscopic properties of four cationic porphyrins possessing phosphoniums residues in the periphery of the porphyrin plane are investigated in aqueous and organic solvent phases. The electronic spectra of the phosphoniumyl porphyrins in pure

Absorption and fluorescence properties of aryl substituted porphyrins in different media

Absorption and fluorescence properties of aryl substituted porphyrins, 5,10,15,20-tetra-4-oxy(aceticacid)phenylporphyrin (TAPP), 5,10,15,20-tetra-(4-phenoxyphenyl) porphyrin (TPPP), 5,10,15,20-tetra-(3-bromo-4-hydroxyphenyl) porphyrin (TBHPP), and 5,10,15

Synthesis and preliminary DNA-interaction studies of a new cationic porphyrin

A new water-soluble porphyrin containing benzyl-trimethylammonium groups was synthesized in a two-step sequence from tetraphenylporphyrin and preliminary studies show that it binds strongly to DNA in an outside manner and gives fairly stable complexes with nucleotides and nucleosides.