173043-61-3

Basic information

• Product Name: Methyl-4,5-dimethoxy-2-iodobenzoate
• Synonyms: Methyl-4,5-dimethoxy-2-iodobenzoate;Methyl 2-iodo-4,5-dimethoxybenzoate;2-Iodo-4,5-dimethoxybenzoic acid methyl ester
• CAS NO: 173043-61-3
• Molecular Formula: C₁₀H₁₁IO₄
• Molecular Weight: 322.09641
• Mol File: 173043-61-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 105-107 °C(Solv: methanol (67-56-1))
• Boiling Point: 352.8±42.0 °C(Predicted)
• Appearance: /
• Density: 1.631±0.06 g/cm3(Predicted)
• Storage Temp.: Refrigerated.
• CAS DataBase Reference: Methyl-4,5-dimethoxy-2-iodobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl-4,5-dimethoxy-2-iodobenzoate(173043-61-3)
• EPA Substance Registry System: Methyl-4,5-dimethoxy-2-iodobenzoate(173043-61-3)

Safety Data

• Hazardous Substances Data: 173043-61-3(Hazardous Substances Data)

Usage

General Description

Methyl-4,5-dimethoxy-2-iodobenzoate is a chemical compound which falls under the category of benzoic acids and derivatives. Its molecular formula is C10H11IO4 and it has a molecular weight of 322.1 g/mol. Methyl-4,5-dimethoxy-2-iodobenzoate is also known by its systematic name, Methyl 2-Iodo-4,5-dimethoxybenzoate. The presence of multiple functional groups like the methoxy group and iodine indicate its potential use in various organic chemistry reactions. Its detailed properties such as boiling point, melting point, and solubility depend on its precise physical state and purity, while specific details about its usage and handling should be referred to in its Material Safety Data Sheet.

Upstream product

• 5653-40-7 2-Amino-4,5-dimethoxybenzoic acid 
• 61203-48-3 2-iodo-4,5-dimethoxybenzoic acid 
• 61203-53-0 2-iodo-4,5-dimethoxybenzaldehyde 
• 67-56-1 methanol 
• 113258-92-7 4,5-dimethoxy-2-iodobenzoyl chloride 
• 93-07-2 Veratric acid 
• 2150-38-1 methyl 3,4-dimethoxybenzoate 

Downstream Products

• 473451-68-2 4,5-dimethoxy-2-(2-nitro-phenylethynyl)-benzoic acid methyl ester 
• 472986-90-6 4,5-dimethoxy-2-styrylbenzoic acid methyl ester 
• 1054471-20-3 2-benzyl-5,6-dimethoxyisoindoline-1,3-dione 
• 548-31-2 oxynitidine 
• 13063-04-2 nitidine chloride 
• 1360789-43-0 methyl 2-((E)-4-hydroxybut-1-enyl)-4,5-dimethoxybenzoate 
• 1637588-34-1 methyl 2-(oct-1-yn-1-yl)-4,5-dimethoxybenzoate 
• 59084-71-8 methyl 2-cyano-4,5-dimethoxybenzoate 
• 61203-48-3 2-iodo-4,5-dimethoxybenzoic acid 
• 120014-06-4 donepezil 
• 1620284-92-5 methyl 4,5-dimethoxy-2-((trifluoromethyl)thio)benzoate 
• 1417741-77-5 2-[(2-ethynyl-4,5-dimethoxyphenyl)ethynyl]-4,5-dimethoxybenzoic acid 
• 1418035-93-4 C₂₂H₂₀O₆ 
• 1360789-84-9 C₂₀H₃₂O₅Si 

Relevant articles and documents

A facile synthesis of dibenzopyrroloazepinones as tetracyclic allocolchicinoids - An unusual 1,2-phenyl shift

A facile synthesis of dibenzopyrroloazepinones via an electrophilic cyclisation of a biphenyl-acyliminium ion is described; an unusual 1,2-phenyl shift occurs when the C-1′ carbon is the more nucleophilic than the C-2′ carbon.

Synthesis of 3-Hexyl-4-cyan-6,7-dimethoxy Isocoumarin

4-(2-Amino-propanamideyl)-3,4,5,6,7,8,9,10-octahydro-5,6, 8-trihydroxy-3-methyl-isocoumarin, which was isolated from Flaveria bidentis (L) Kuntze, had herbicidal activity and its structure was modified in this research in order to get the isocoumarin comp

Heck-mediated synthesis and photochemically induced cyclization of [2-(2-styrylphenyl)ethyl]carbamic acid ethyl esters and 2-styryl-benzoic acid methyl esters: Total synthesis of naphtho[2,1f]isoquinolines (2-azachrysenes)

We describe two new closely related total syntheses of naphtho[2,1-f]isoquinolines. The first synthesis consists of a Heck coupling reaction between trifluoromethanesulfonic acid 2-(2-ethoxycarbonylaminoethyl)phenyl esters and styrenes to give [2-(2-styrylphenyl)ethyl]carbamic acid ethyl esters. These compounds cyclize to give (2-phenanthren-1-yl-ethyl)carbamic acid ethyl esters, from which 2-azachrysenes can be obtained in a three-step sequence. The second synthesis includes a new total synthesis of 2-styrylbenzoic acid methyl esters by Heck coupling of methyl o-iodobenzoates to styrenes, followed by the transformation of the resulting benzoic acid derivatives into phenanthrene-1-carboxylic acid methyl esters and then into the target compounds by a six-step sequence including a Bischler-Napieralski cyclization.