129997-27-9

Basic information

• Product Name: (trans-dibenzoato)(5,10,15,20-tetraphenylporphyrinato)tin(IV)
• Synonyms: (trans-dibenzoato)(5,10,15,20-tetraphenylporphyrinato)tin(IV)
• CAS NO: 129997-27-9
• Molecular Weight: 973.674
• Mol File: 129997-27-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (trans-dibenzoato)(5,10,15,20-tetraphenylporphyrinato)tin(IV)(CAS DataBase Reference)
• NIST Chemistry Reference: (trans-dibenzoato)(5,10,15,20-tetraphenylporphyrinato)tin(IV)(129997-27-9)
• EPA Substance Registry System: (trans-dibenzoato)(5,10,15,20-tetraphenylporphyrinato)tin(IV)(129997-27-9)

Safety Data

• Hazardous Substances Data: 129997-27-9(Hazardous Substances Data)

Upstream product

• 26334-89-4 trans-dihydroxo(meso-tetraphenylporphyrinato)tin(IV) 
• 13988-67-5 benzoylpivaloylmethane 
• 93-91-4 1-phenylbutan-1,3-dione 
• 120-46-7 1,3-diphenylpropanedione 
• 65-85-0 benzoic acid 
• 874947-50-9 [(tetraphenylporphyrin)Sn(IV)(OSi(O-tert-Bu)3)2] 

Downstream Products

• 26334-89-4 trans-dihydroxo(meso-tetraphenylporphyrinato)tin(IV) 

Relevant articles and documents

Sn(IV) Multiporphyrin Arrays as Tunable Photoactive Systems

A series of four arrays made of a central Sn(IV) porphyrin as scaffold axially connected, via carboxylate functions, to two free-base porphyrins has been prepared and fully characterized. Three arrays in the series feature the same free-base unit and alte

Synthesis of calix[4]arene-bis(tin(IV)porphyrins) and supramolecular complexes on their basis

Selective substitution of one of the two trans hydroxy groups of calix[4]arene-bis(porphyrinato-tin(IV)) resulted in supramolecular tetramer assemblies based thereon with parallel and perpendicular arrangement of tetrapyrrole macrocyclic rings, which were characterized by UV spectroscopy, 1H NMR, and elemental analysis data.

Efficient formation of lipophilic dihydroxotin(IV) porphyrins and bis-porphyrins

Treatment of dichloro- and dicarboxylato-tin(IV) porphyrins with K2CO3 in THF-H2O (4 : 1) is a mild and highly efficient method for formation of dihydroxotin(IV) porphyrins; unlike other reported procedures, this method is