23602-64-4

Basic information

• Product Name: 3-Iodo-2-hydroxybenzaldehyde
• Synonyms: 2-Hydroxy-3-iodobenzaldehyde;3-Iodo-2-hydroxybenzaldehyde;3-Iodosalicylaldehyde
• CAS NO: 23602-64-4
• Molecular Formula: C₇H₅IO₂
• Molecular Weight: 248.014
• Mol File: 23602-64-4.mol
• Article Data: 9

Chemical Properties

• Melting Point: 69-71 ºC
• Boiling Point: 216 ºC
• Flash Point: 84 ºC
• Appearance: /
• Density: 2.039
• Vapor Pressure: 0.0985mmHg at 25°C
• Refractive Index: 1.715
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• PKA: 6.72±0.10(Predicted)
• CAS DataBase Reference: 3-Iodo-2-hydroxybenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Iodo-2-hydroxybenzaldehyde(23602-64-4)
• EPA Substance Registry System: 3-Iodo-2-hydroxybenzaldehyde(23602-64-4)

Safety Data

• Hazardous Substances Data: 23602-64-4(Hazardous Substances Data)

Usage

Description

3-Iodo-2-hydroxybenzaldehyde is an organic compound that features a benzene ring with a hydroxyl group at the 2nd position and an iodine atom at the 3rd position. It is known for its reactivity and is commonly utilized in various chemical processes and organic synthesis.

Uses

Used in Organic Synthesis:
3-Iodo-2-hydroxybenzaldehyde is used as a reagent for organic synthesis due to its unique structure and reactivity. It serves as a key intermediate in the creation of various complex organic molecules and compounds.
Used in Chemical Processes:
In the chemical industry, 3-Iodo-2-hydroxybenzaldehyde is employed as a reagent in different chemical processes. Its iodine and hydroxyl functional groups make it a versatile building block for the development of new materials and compounds with specific properties and applications.

InChI:InChI=1/C7H5IO2/c8-6-3-1-2-5(4-9)7(6)10/h1-4,10H

Upstream product

• 67-66-3 chloroform 
• 533-58-4 2-Iodophenol 
• 50-00-0 formaldehyd 
• 848890-10-8 7-iodo-2-trimethylsilylbenzofuran 
• 444095-29-8 2-hydroxy-3-(trimethylsilyl)benzaldehyde 
• 271-89-6 1-benzofurane 
• 60981-57-9 (benzofuran-2-yl)trimethylsilane 
• 90-02-8 salicylaldehyde 

Downstream Products

• 473918-96-6 2-benzyloxy-3-iodo-benzoic acid 2-trimethylsilanyl-ethyl ester 
• 473918-97-7 4-[2-benzyloxy-3-(2-trimethylsilanyl-ethoxycarbonyl)-phenyl]-3-formyl-indole-1-carboxylic acid benzyl ester 
• 874347-49-6 3-iodo-2-methoxy-benzaldehyde 
• 128033-28-3 methyl 2-hydroxy-3-iodobenzoate 
• 1385774-61-7 9-(2-(2,4-difluorophenyl)ethynyl)-3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-one 
• 1385774-62-8 10-(2-(2,4-difluorophenyl) ethynyl)-2,3,4,5-tetrahydrobenzo [b][1,5]oxazocin-6-one 
• 1385774-65-1 (R)-2-(9-((2,4-difluorophenyl)ethynyl)-5-oxo-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepine-4-carboxamido)-3-(isobutylthio)propanoic acid 
• 1385774-67-3 (R)-2-(10-((2,4-difluorophenyl)ethynyl)-6-oxo-3,4,5,6-tetrahydro-2H-benzo[b][1,5]oxazocine-5-carboxamido)-3-(isobutylthio)propanoic acid 
• 1385774-56-0 C₁₅H₂₀INO₅ 

Relevant articles and documents

Microwave synthesis and crystal structure of 2-hydroxy-3-iodobenzaldehyde- copper (II)

One new complex, 2-hydroxy-3-iodo-benzaldehyde-copper (II) has been designed and microwave synthesized. The structure was determined by UV, IR and single X-ray crystallography study. The title complex C14H 8CuI2O4 crystallizes in the orthorhombic space group Pna21 with the cell parameters a = 12.7897(12) A, b = 6.1132(8) A, c = 19.5114(18) A, V = 1525.5(3) A3 and Z = 4. The central copper (II) is four-coordinated by four oxygen atoms from two 3-iodosalicylaldehyde. The complex is linked into rhombic crystals by weak intermolecular interactions. Springer Science+Business Media, LLC 2010.

Diversely halogenated spiropyrans - Useful synthetic building blocks for a versatile class of molecular switches

Spiropyrans are dyes that can be reversibly switched to a highly colored merocyanine form by a number of stimuli such as light, mechanical force or temperature. To make use of these molecules, there is a requirement to functionalize them appropriately. Herein we report a library of spiropyrans bearing two (pseudo) halide functional groups on either half of the molecule. Such halide substituents are valuable, because they themselves may be used as reactive sites in cross-coupling reactions, for example. Different combinations of halides, for which different reactivities in cross-coupling reactions may be expected, will facilitate selective consecutive cross-coupling reactions and condensations. Data concerning the UV/vis characteristics, the photostationary equilibria of the materials as well as the half-life of the merocyanine forms in solution are presented.

OLIGOMERISATION OF ETHYLENE TO MIXTURES OF 1-HEXENE AND 1-OCTENE

A process for the oligomerisation, preferably the tetramerisation, of ethylene to predominantly 1- hexene or 1-octene or mixtures of 1-hexene and 1-octene includes contacting ethylene with a catalyst under ethylene oiigomerisation conditions. The catalyst