18179-39-0

Basic information

• Product Name: METHYL 4-IODOSALICYLATE
• Synonyms: Methyl 2-Hydroxy-4-iodobenzoate 4-Iodosalicylic Acid Methyl Ester 2-Hydroxy-4-iodobenzoic Acid Methyl Ester;Methyl 4-iodosalicylate, 5-Iodo-2-(methoxycarbonyl)phenol;Methyl 4-iodosalicylate 97%;Methyl4-Iodosilicylate;2-Hydroxy-4-iodobenzoic Acid Methyl Ester;4-Iodosalicylic Acid Methyl Ester
• CAS NO: 18179-39-0
• Molecular Formula: C₈H₇IO₃
• Molecular Weight: 278.11925
• Mol File: 18179-39-0.mol
• Article Data: 12

Chemical Properties

• Melting Point: 69-73 °C
• Boiling Point: 309.7 °C at 760 mmHg
• Flash Point: 141.1 °C
• Appearance: /
• Density: 1.88 g/cm³
• Vapor Pressure: 0.000344mmHg at 25°C
• Refractive Index: 1.633
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 8.91±0.10(Predicted)
• Sensitive: Light Sensitive
• CAS DataBase Reference: METHYL 4-IODOSALICYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 4-IODOSALICYLATE(18179-39-0)
• EPA Substance Registry System: METHYL 4-IODOSALICYLATE(18179-39-0)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 45
• RIDADR: UN 2811 6.1/PG 3
• WGK Germany: 3
• F: 8
• PackingGroup: III
• Hazardous Substances Data: 18179-39-0(Hazardous Substances Data)

Usage

General Description

Methyl 4-Iodosalicylate is a chemical compound with the formula C8H7IO3. It is classified as an ester, which are often derived from carboxylic acids and alcohols. Methyl 4-Iodosalicylate exhibits an iodine substitution at the 4-position of the salicylate structure. It is used primarily as a reagent in various organic synthesizing processes, particularly in pharmaceuticals manufacturing. Like many compounds, handling it may require care as it may pose health risks if improperly managed. The compound's properties make it an integral part in the chemistry field, especially in the creation of other complex compounds.

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

Upstream product

• 67-56-1 methanol 
• 16870-28-3 4-iodosalicylic acid 
• 74-88-4 methyl iodide 
• 65-49-6 4-Aminosalicylic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 4136-97-4 methyl 4-aminosalicylate 
• 124-41-4 sodium methylate 

Downstream Products

• 170355-72-3 methyl 2-hydroxy-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)benzoate 
• 184533-27-5 methyl 2-hydroxy-4-[7-(1-adamantyl)-6-benzyloxy-2-naphthyl]benzoate 
• 1246765-31-0 methyl 2-ethoxy-4-iodobenzoate 
• 1275536-04-3 methyl 2-acetoxy-4-iodobenzoate 
• 1579939-88-0 4-[2-(4-carboxy-3-hydroxy-phenyl)ethynyl]-2-hydroxy-benzoic acid 
• 1579939-89-1 4-[4-(4-carboxy-3-hydroxy-phenyl)buta-1,3-diynyl]-2-hydroxy-benzoic acid 
• 1579939-84-6 C₂₀H₂₂O₃Si 
• 1579939-85-7 C₁₇H₁₄O₃ 
• 1579939-86-8 dimethyl 4,4′-(ethyne-1,2-diyl)bis(2-(benzyloxy)benzoate) 
• 1608471-45-9 (R)-4-(1-(4-cyano-3-methylphenyl)-5-cyclopentyl-4,5-dihydro-1H-pyrazol-3-yl)-2-ethoxybenzoic acid 
• 851334-98-0 methyl 2-ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 

Relevant articles and documents

Three-Dimensional Porous Architectures Based on MnII/III Three-Blade Paddle Wheel Metallacryptates

Three metallacryptate supramolecular assemblies have been obtained using salicylhydroxamic acid derivatives (H3L). The three ligands differ in the residue at the para position with respect to the hydroxamic function (-H, -NH2, and -(

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Synthesis and antioxidant effect of caffeic acid analogues bearing a carboxy and hydroxymethyl group

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