1229403-09-1

Basic information

• Product Name: 3,4-dihydroxy-2-iodobenzaldehyde
• Synonyms: 3,4-dihydroxy-2-iodobenzaldehyde
• CAS NO: 1229403-09-1
• Molecular Weight: 264.019
• Mol File: 1229403-09-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,4-dihydroxy-2-iodobenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-dihydroxy-2-iodobenzaldehyde(1229403-09-1)
• EPA Substance Registry System: 3,4-dihydroxy-2-iodobenzaldehyde(1229403-09-1)

Safety Data

• Hazardous Substances Data: 1229403-09-1(Hazardous Substances Data)

Upstream product

• 621-59-0 isovanillin 
• 138490-94-5 2-iodoisovanillin 

Downstream Products

• 1440546-85-9 methyl 2-iodo-3,4-diisobutoxybenzoate 
• 1440546-86-0 methyl 2-((2-amino-5-(benzyloxy)phenyl)ethynyl)-3,4-diisobutoxybenzoate 
• 1440546-87-1 tert-Butyl (2-(2-((2-amino-5-(benzyloxy)phenyl)ethynyl)-3,4-diisobutoxybenzamido) ethyl)carbamate 
• 1440546-88-2 ethyl2-((4-(benzyloxy)-2-((6-((2-((tert-butoxycarbonyl)amino)ethyl)carbamoyl)-2,3diisobutoxyphenyl)ethynyl)phenyl)amino)-2-oxoacetate 
• 1440546-81-5 2-((2-((6-((2-aminoethyl)carbamoyl)-2,3-diisobutoxyphenyl)ethynyl)-4-(benzyloxy)phenyl)amino)-2-oxoaceticacid 
• 1440546-90-6 2-iodo-3,4-diisobutoxybenzoic acid 
• 1440546-91-7 2-((2-amino-5-(benzyloxy)phenyl)ethynyl)-3,4-diisobutoxybenzoic acid 
• 1440546-93-9 2-((4-(benzyloxy)-2-((6-((2-((tert-butoxycarbonyl)amino)ethyl)carbamoyl)-2,3-diisobutoxyphenyl)ethynyl)phenyl)amino)-2-oxoacetic acid 
• 1440546-84-8 2-iodo-3,4-diisobutoxybenzaldehyde 

Relevant articles and documents

Amphipathic α-helix mimetics based on a 1,2-diphenylacetylene scaffold

In order to mimic amphipathic α-helices, a novel scaffold based on a 1,2-diphenylacetylene was designed. NMR and computational modeling confirmed that an intramolecular hydrogen bond favors conformations of the 1,2-diphenylacetylene that allow for accurat

Cyclopropylmethyl Protection of Phenols: Total Synthesis of the Resveratrol Dimers Anigopreissin A and Resveratrol–Piceatannol Hybrid

We demonstrate the versatile use of the cyclopropylmethyl group to protect phenols through the total synthesis of two benzofuran-based natural products, that is, anigopreissin A and the resveratrol–piceatannol hybrid. This protecting group is a good alter