15126-06-4

Basic information

• Product Name: METHYL 4-HYDROXY-3-IODOBENZOATE
• Synonyms: METHYL 4-HYDROXY-3-IODOBENZOATE;4-HYDROXY-3-IODOBENZOIC ACID METHYL ESTER;Methyl 3-Iodo-4-hydroxybenzoate;2-Iodo-4-(methoxycarbonyl)phenol;Methyl 4-hydroxy-3-iodobenzoate 97%
• CAS NO: 15126-06-4
• Molecular Formula: C₈H₇IO₃
• Molecular Weight: 278.04
• Product Categories: C8 to C9;Carbonyl Compounds;Esters
• Mol File: 15126-06-4.mol
• Article Data: 30

Chemical Properties

• Melting Point: 155-159 °C(lit.)
• Boiling Point: 292.7 °C at 760 mmHg
• Flash Point: 130.8 °C
• Appearance: White to pale brown/Crystal or Powder
• Density: 1.88 g/cm³
• Vapor Pressure: 0.00103mmHg at 25°C
• Refractive Index: 1.633
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• PKA: 6.91±0.18(Predicted)
• Sensitive: Light Sensitive
• CAS DataBase Reference: METHYL 4-HYDROXY-3-IODOBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 4-HYDROXY-3-IODOBENZOATE(15126-06-4)
• EPA Substance Registry System: METHYL 4-HYDROXY-3-IODOBENZOATE(15126-06-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-41
• Safety Statements: 26-39
• WGK Germany: 3
• Hazardous Substances Data: 15126-06-4(Hazardous Substances Data)

Usage

Chemical Properties

Off White Powder

InChI:InChI=1/C8H7IO3/c1-12-8(11)5-2-3-7(10)6(9)4-5/h2-4,10H,1H3

Upstream product

• 37470-46-5 4-hydroxy-3-iodobenzoic acid 
• 74-88-4 methyl iodide 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 99-96-7 4-hydroxy-benzoic acid 
• 1571-72-8 3-amino-4-hydroxybenzoic acid 
• 4253-10-5 methyl 3,5-diiodo-4-methoxybenzoate 
• 3337-66-4 methyl 4-hydroxy-3,5-diiodobenzoate 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 32294-60-3 diphenyl ditelluride 
• 67-56-1 methanol 

Downstream Products

• 195060-55-0 3-iodo-4-[2-oxo-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-ethoxy]benzoic acid methyl ester 
• 207865-33-6 4-[2-(3-Adamantan-1-yl-4-methoxy-phenyl)-2-oxo-ethoxy]-3-iodo-benzoic acid methyl ester 
• 207865-34-7 methyl 4-[2-(8,8-dimethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-2-oxoethoxy]-3-iodobenzoate 
• 207865-35-8 Methyl 3-iodo-4-[2-oxo-2-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethoxy]-benzoate 
• 551002-32-5 methyl 2-(4-methoxyphenyl)benzofuran-5-carboxylate 
• 501892-55-3 methyl 4-hydroxy-3-((trimethylsilyl)-ethynyl)benzoate 
• 401928-89-0 methyl 2-[4-(tert-butyldiphenylsilanyloxy)butyl]benzofuran-5-carboxylate 
• 167550-87-0 methyl 4-hydroxy-3-cyclopentylbenzoate 
• 588703-25-7 C₁₃H₁₅IO₃ 
• 1202754-31-1 methyl 3-(3,4-dimethoxybenzyl)-5-oxo-4-tosyl-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepine-7-carboxylate 
• 197230-74-3 4-(hydroxymethyl)-2-iodophenol 

Relevant articles and documents

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Palladium-Catalyzed Chemoselective Oxidative Addition of Allyloxy-Tethered Aryl Iodides: Synthesis of Medium-Sized Rings and Mechanistic Studies

This Letter describes a Pd-catalyzed Tsuji-Trost-type/Heck reaction with allyloxy-tethered aryl iodides and aziridines. The strategy provides efficient access to benzannulated medium-sized rings via intermolecular cyclization. The substrate aryl iodide ha

Efficient and sustainable laccase-catalyzed iodination of: P -substituted phenols using KI as iodine source and aerial O2 as oxidant

The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mild reaction conditions.