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

Description

Methyl 4-Iodosalicylate, with the chemical formula C8H7IO3, is an ester compound derived from the combination of a carboxylic acid and an alcohol. It features an iodine atom substitution at the 4-position of the salicylate structure, which contributes to its unique properties and applications in the chemical and pharmaceutical fields.

Uses

Used in Pharmaceutical Industry:
Methyl 4-Iodosalicylate is used as a reagent for the synthesis of various pharmaceutical compounds. Its iodine substitution at the 4-position allows for the creation of complex molecules that can be utilized in the development of new drugs and medications.
Used in Organic Synthesis:
In the field of organic chemistry, Methyl 4-Iodosalicylate serves as a key intermediate in the synthesis of other complex organic compounds. Its unique structure and reactivity make it a valuable component in the preparation of a wide range of chemical products.

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 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 124-41-4 sodium methylate 
• 65-49-6 4-Aminosalicylic acid 
• 4136-97-4 methyl 4-aminosalicylate 
• 74-88-4 methyl iodide 

Downstream Products

• 217818-09-2 methyl 2-hydroxy-4-[3-hydroxy-3-(4,4-dimethylchroman-8-yl)prop-1-ynyl]benzoate 
• 16870-28-3 4-iodosalicylic acid 
• 854028-39-0 methyl 2-heptyloxy-4-iodobenzoate 
• 854028-45-8 methyl 4-iodo-2-phenethyloxybenzoate 
• 170100-60-4 methyl 4-trimethylsilanylethynyl-2-hydroxybenzoate 
• 166386-81-8 2-Hydroxy-4-iodo-benzylalcohol 
• 148490-97-5 4-iodo-2-methoxybenzoic acid-methyl ester 
• 170100-43-3 methyl 4-[3-hydroxy-3-(3,tert-butyl-4-methoxyphenyl)-1-propynyl]benzoate 
• 854028-46-9 methyl 2-(benzyloxy)-4-iodobenzoate 
• 1224717-24-1 {4-[2-(4-ethoxyphenyl)ethyl]-2-(methoxymethoxy)phenyl}methanol 
• 1224717-25-2 4-[2-(4-ethoxyphenyl)ethyl]-2-(methoxymethoxy)benzaldehyde 
• 1224717-26-3 4-[2-(4-ethoxyphenyl)ethyl]-2-hydroxybenzaldehyde 
• 1224717-27-4 1-{6-[2-(4-ethoxyphenyl)ethyl]-1-benzofuran-2-yl}ethanone 

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 -(

Acetylene Bridged Linkers and Metal-Organic Frameworks (MOFs) Produced Thereof

Described are acetylene bridged linkers, metal-organic frameworks produced thereof, processes for producing the linkers and the metal-organic frameworks, and the use of the metal-organic frameworks. The metal-organic frameworks possess an enhanced ability to adsorb and desorb high amounts of gases, in particular methane or hydrogen. The metal-organic frameworks have a high porosity and, thus, a high inner surface.

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

-