19337-60-1

Basic information

• Product Name: 3-Iodcatechol
• Synonyms: 3-Iodcatechol;3-Iodobenzene-1,2-diol;3-iodo-1,2-benzenediol
• CAS NO: 19337-60-1
• Molecular Formula: C₆H₅IO₂
• Molecular Weight: 236.00717
• Mol File: 19337-60-1.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 3-Iodcatechol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Iodcatechol(19337-60-1)
• EPA Substance Registry System: 3-Iodcatechol(19337-60-1)

Safety Data

• Hazardous Substances Data: 19337-60-1(Hazardous Substances Data)

Usage

General Description

3-Iodcatechol, also known as 3-iodo-1,2-dihydroxybenzene, is a chemical compound with the molecular formula C6H5IO2. It is derived from catechol, a benzene diol, by the replacement of one of the hydroxyl groups with an iodine atom. 3-Iodcatechol is commonly used as a reagent in organic synthesis, particularly in the preparation of various pharmaceutical intermediates. It is also utilized in the production of dyes and pigments. This chemical has been found to exhibit moderate cytotoxicity toward cancer cells, making it a potential candidate for anticancer drug development. However, due to its potential hazards, 3-Iodcatechol should be handled with caution and appropriate safety measures.

Upstream product

• 626-02-8 3-Iodophenol 
• 91-16-7 1,2-dimethoxybenzene 
• 591-50-4 iodobenzene 
• 25245-33-4 1-iodo-2,3-dimethoxybenzene 
• 138769-92-3 cis-(1S,2S)-1,2-dihydroxy-3-iodocyclohexa-3,5-diene 

Downstream Products

• 1010685-17-2 C₃₀H₅₃IO₂ 
• 113678-91-4 di-hydroxyphenyl-ethylene 
• 67984-81-0 2,3-dihydroxybenzonitrile 
• 1133-63-7 3-phenylcatechol 
• 2411-83-8 methyl-2,3-dihydroxybenzoate 
• 1607814-83-4 2-iodo-6-(oxan-2-yloxy)phenol 
• 1607814-73-2 2-iodo-6-(oxan-2-yloxy)phenyl methyl carbonate 
• 1607814-79-8 methyl 2-[2-(methoxymethoxy)phenyl]-8-(oxan-2-yloxy)-4-oxo-4H-chromene-3-carboxylate 
• 1607814-76-5 2-{3-[2-(methoxymethoxy)phenyl]prop-2-ynoyl}-6-(oxan-2-yloxy)phenyl methyl carbonate 
• 1444011-07-7 C₂₀H₁₇IO₂ 
• 1444011-04-4 C₃₄H₃₈O₆ 
• 1444011-10-2 C₅₈H₆₂O₆ 
• 1444011-09-9 C₂₆H₂₉BO₄ 

Relevant articles and documents

Enzyme-Catalysed Synthesis of Cyclohex-2-en-1-one cis-Diols from Substituted Phenols, Anilines and Derived 4-Hydroxycyclohex-2-en-1-ones

Toluene dioxygenase-catalysed cis-dihydroxylations of substituted aniline and phenol substrates, with a Pseudomonas putida UV4 mutant strain and an Escherichia coli pCL-4t recombinant strain, yielded identical arene cis-dihydrodiols, which were isolated as the preferred cyclohex-2-en-1-one cis-diol tautomers. These cis-diol metabolites were predicted by preliminary molecular docking studies, of anilines and phenols, at the active site of toluene dioxygenase. Further biotransformations of cyclohex-2-en-1-one cis-diol and hydroquinone metabolites, using Pseudomonas putida UV4 whole cells, were found to yield 4-hydroxycyclohex-2-en-1-ones as a new type of phenol bioproduct. Multistep pathways, involving ene reductase- and carbonyl reductase-catalysed reactions, were proposed to account for the production of 4-hydroxycyclohex-2-en-1-one metabolites. Evidence for the phenol hydrate tautomers of 4-hydroxycyclohex-2-en-1-one metabolites was shown by formation of the corresponding trimethylsilyl ether derivatives. (Figure presented.).

Discrete, soluble covalent organic boronate ester rectangles

The facile self-assembly of nanoscale boronate ester rectangles from linear bis-catechols and 1,4-benzene diboronic acid is described. Spectroscopic and computational analyses reveal the influence of extended π-conjugation on the rectangles' absorption an

Columnar mesophases from half-discoid platinum cyclometalated metallomesogens

A series of liquid crystals have been synthesized and studied based upon mononuclear ortho-platinated rod-like heteroaromatic and 1,3-diketonate ligands. The liquid crystalline properties of these molecules were investigated using polarized light optical