62672-58-6

Basic information

• Product Name: 3-HYDROXY-2-IODOBENZALDEHYDE
• Synonyms: 3-HYDROXY-2-IODOBENZALDEHYDE;H90001;Benzaldehyde, 3-hydroxy-2-iodo-
• CAS NO: 62672-58-6
• Molecular Formula: C₇H₅IO₂
• Molecular Weight: 248.014
• Product Categories: Aromatic Aldehydes & Derivatives (substituted)
• Mol File: 62672-58-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-HYDROXY-2-IODOBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-HYDROXY-2-IODOBENZALDEHYDE(62672-58-6)
• EPA Substance Registry System: 3-HYDROXY-2-IODOBENZALDEHYDE(62672-58-6)

Safety Data

• Hazardous Substances Data: 62672-58-6(Hazardous Substances Data)

Upstream product

• 70738-03-3 2-iodo-3-methoxybenzaldehyde 
• 100-83-4 meta-hydroxybenzaldehyde 
• 6971-51-3 3-methoxybenzyl alcohol 
• 162136-06-3 (2-iodo-3-methoxyphenyl)methanol 

Downstream Products

• 303-38-8 2,3-Dihydroxybenzoic acid 
• 75821-44-2 3-hydroxy-2-iodobenzoic acid 
• 704892-59-1 4,6-dibromo-3-hydroxy-2-iodo-benzaldehyde 
• 860562-84-1 3-acetoxy-2-iodo-benzoic acid 
• 53872-06-3 2,4-dibromo-6-iodophenol 
• 1004761-02-7 3,3'-{[(2R,3R)-1,4-bis(benzyloxy)butane-2,3-diyl]bis(oxy)}bis(2-iodobenzaldehyde) 
• 1352212-87-3 (2S,4S)-1-(3-(allyloxy)-2-iodobenzyl)-4-(tert-butyldimethylsilyloxy)-N-methyl-N-phenyl-pyrrolidine-2-carboxamide 
• 1352212-89-5 (2S,10S,10aS)-9-allyloxy-10-benzoyloxy-2-hydroxy-1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinoline 
• 1352212-94-2 (2S,10S,10aS)-9-allyloxy-10-benzoyloxy-1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinolin-2-yl (2'R,3'S)-3'-benzoylamino-2'-hydroxy-3'-(2-(allyloxy)phenyl)-propanoate 
• 1352212-93-1 (2S,10S,10aS)-9-allyloxy-10-benzoyloxy-1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinolin-2-yl (2'R,3'S)-3'-benzoylamino-2'-hydroxy-3'-(2-(but-3-enyloxy)phenyl)-propanoate 
• 1352212-95-3 (2S,10S,10aS)-9-allyloxy-10-benzoyloxy-1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinolin-2-yl (2'R,3'S)-3'-benzoylamino-2'-hydroxy-3'-(2-allylphenyl)-propanoate 
• 1352212-96-4 (2S,10S,10aS)-9-allyloxy-10-hydroxy-1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinolin-2-yl (2'R,3'S)-3'-benzoylamino-2'-triisopropylsilyloxy-3'-(2-(but-3-enyloxy)phenyl)-propanoate 
• 1352212-97-5 (2S,10S,10aS)-9-allyloxy-10-hydroxy-1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinolin-2-yl (2'R,3'S)-3'-benzoylamino-2'-triisopropylsilyloxy-3'-(2-(allyloxy)phenyl)-propanoate 
• 1352212-98-6 (2S,10S,10aS)-9-allyloxy-10-hydroxy-1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinolin-2-yl (2'R,3'S)-3'-benzoylamino-2'-triisopropylsilyloxy-3'-(2-allylphenyl)-propanoate 

Relevant articles and documents

Scalable Biomimetic Syntheses of Paeciloketal B, 1- epi-Paeciloketal B, and Bysspectin A

The first total synthesis of the benzannulated 5,5-spiroketal natural products paeciloketal B and 1-epi-paeciloketal B has been achieved in 10 linear steps employing a biomimetic spiroketalization. This approach also furnished the related natural product

In vitro photodynamic activity of 5,15-bis(3-Hydroxyphenyl)porphyrin and its halogenated derivatives against cancer cells

5,15-Diarylporphyrins (1-5) with hydroxyl groups and halogens as substituents were prepared by condensation between unsubstituted dipyrromethane and halogenated m-hydroxybenzaldehydes. Photophysical properties show that the nonhalogenated porphyrin 1 has higher fluorescence yield but lower singlet oxygen formation quantum yield than the halogenated derivatives due to the heavy atom effect. The in vitro activity of these derivatives was tested against WiDr colorectal adenocarcinoma and A375 melanoma cancer cells. All porphyrins present a much higher phototoxicity than Photofrin with IC 50 values lower than the 50 nm level for WiDr cells and 25 nm level for A375 cancer cells. The most photoactive compound is the nonhalogenated porphyrin 1 which also presents the highest uptake. Halogenated derivatives present much lower uptakes than 1. However, their photoactivity is similar to compound 1 showing that their intrinsic photoactivity (ISP) is very high. Iodinated compound 4 presents the highest ISP. The greater ability of these porphyrins to destroy cancer cells could be related to their photophysical and photochemical properties.