106456-88-6

Basic information

• Product Name: Benzaldehyde, 4-(5,5-dimethyl-1,3-dioxan-2-yl)-
• Synonyms: Benzaldehyde, 4-(5,5-dimethyl-1,3-dioxan-2-yl)-
• CAS NO: 106456-88-6
• Molecular Formula: C₁₃H₁₆O₃
• Molecular Weight: 220
• Mol File: 106456-88-6.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzaldehyde, 4-(5,5-dimethyl-1,3-dioxan-2-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-(5,5-dimethyl-1,3-dioxan-2-yl)-(106456-88-6)
• EPA Substance Registry System: Benzaldehyde, 4-(5,5-dimethyl-1,3-dioxan-2-yl)-(106456-88-6)

Safety Data

• Hazardous Substances Data: 106456-88-6(Hazardous Substances Data)

Upstream product

• 623-27-8 terephthalaldehyde, 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 2591-86-8 N-Formylpiperidine 
• 105114-53-2 1-bromo-4-(5,5-dimethyl-1,3-dioxan-2-yl)benzene 
• 1571-08-0 methyl 4-formylbenzoate 
• 138536-73-9 4-(5,5-Dimethyl-[1,3]dioxan-2-yl)-benzoic acid methyl ester 
• 105-07-7 4-cyanobenzaldehyde 
• 1122-91-4 4-bromo-benzaldehyde 
• 68-12-2 N,N-dimethyl-formamide 
• 127462-96-8 [4-(5,5-Dimethyl-[1,3]dioxan-2-yl)-phenyl]-methanol 
• 106456-92-2 p-formylbenzonitrile neopentyl glycol acetal 

Downstream Products

• 106456-80-8 meso-tetrakis<4-(1,3-dioxa-5,5-dimethylcyclohex-2-yl)phenyl>porphyrin 
• 150805-46-2 5,10,15,20-tetrakis(4-formylphenyl)-21H,23H-porphyrin 
• 137709-20-7 C₁₄₀H₁₉₆N₈O₆ 
• 133528-27-5 C₉₂H₉₆N₈O₃ 
• 131531-55-0 5,15-Bis(4-formylphenyl)-2,8,12,18-tetraethyl-3,7,13,17-tetramethylporphine 
• 133528-26-4 4-{(1Z,4Z,9Z,15Z)-15-[4-(2,5-Dimethoxy-benzyl)-phenyl]-2,8,12,18-tetraethyl-3,7,13,17-tetramethyl-porphyrin-5-yl}-benzaldehyde 
• 133528-25-3 (5Z,10Z,14Z,19Z)-5,15-Bis-[4-(2,5-dimethoxy-benzyl)-phenyl]-2,8,12,18-tetraethyl-3,7,13,17-tetramethyl-porphyrin 

Relevant articles and documents

Synthesis, spectroscopic properties and photodynamic activity of porphyrin-fullerene C60 dyads with application in the photodynamic inactivation of Staphylococcus aureus

A covalently linked porphyrin-fullerene C60 dyad 5 was synthesized by 1,3-dipolar cycloaddition using 5-(4-formylphenyl)-10,15,20- tris[3-(N-ethylcarbazoyl)]porphyrin, N-methylglycine and fullerene C 60. Methylation of 5 was used to

Synthesis and spectroscopic properties of a covalently linked porphyrin-fullerene C60 dyad

A covalently linked porphyrin-fullerene C 60 dyad 6 was conveniently synthesized by 1,3-dipolar cycloaddition using 5-(4-carbonylphenyl)-10,15,20- tris(4-methoxylphenyl)porphyrin 5, N -methylglycine and fullerene C 60 . Spectroscopic studies show that dya

Mild water-promoted selective deacetalisatison of acyclic acetals

Various aliphatic and aromatic dimethyl and diethyl acetals and ketals were found to hydrolyse in essentially quantitative yield when heated to 80 °C in neat water or aqueous medium without a catalyst or any other additive, while cyclic acetals were stable under these conditions. Selective deprotection is possible when both types of acetal are present. The Royal Society of Chemistry 2010.