96122-61-1

Basic information

• Product Name: (3-IODO-4-METHOXYPHENYL)ACETIC ACID
• Synonyms: (3-IODO-4-METHOXYPHENYL)ACETIC ACID
• CAS NO: 96122-61-1
• Molecular Formula: C₉H₉IO₃
• Molecular Weight: 292.07
• Mol File: 96122-61-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3-IODO-4-METHOXYPHENYL)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (3-IODO-4-METHOXYPHENYL)ACETIC ACID(96122-61-1)
• EPA Substance Registry System: (3-IODO-4-METHOXYPHENYL)ACETIC ACID(96122-61-1)

Safety Data

• Hazardous Substances Data: 96122-61-1(Hazardous Substances Data)

Usage

Description

(3-IODO-4-METHOXYPHENYL)ACETIC ACID is a chemical compound with the molecular formula C9H9IO3. It is an organic compound that belongs to the class of acetic acid derivatives. (3-IODO-4-METHOXYPHENYL)ACETIC ACID contains a phenyl ring substituted with both a methoxy group and an iodo group, attached to an acetic acid moiety. It is commonly used in the synthesis of pharmaceuticals and other organic compounds.

Uses

Used in Pharmaceutical Industry:
(3-IODO-4-METHOXYPHENYL)ACETIC ACID is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its ability to modulate biological pathways and target specific receptors makes it a valuable component in drug development.
Used in Medicinal Chemistry:
(3-IODO-4-METHOXYPHENYL)ACETIC ACID is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and functional groups allow for the development of new compounds with potential applications in medicinal chemistry.

Upstream product

• 104-01-8 4-Methoxyphenylacetic acid 

Downstream Products

• 96122-62-2 <3-(2-carboxyphenylthio)-4-methoxyphenyl>acetic acid 
• 124840-58-0 3-Iod-4-methoxy-phenylessigsaeure-methylester 
• 185200-34-4 (3-Iodo-4-methoxy-phenyl)-acetic acid benzyl ester 
• 96122-63-3 <3-(2-carboxyphenylthio)-4-hydroxyphenyl>acetic acid 
• 96122-65-5 <4-acetoxy-2-(2-carboxyphenylthio)phenyl>acetic acid 
• 857570-90-2 C₉H₈ClIO₂ 

Relevant articles and documents

One-pot ortho-amination of aryl C-H bonds using consecutive iron and copper catalysis

A one-pot approach for ortho-coupling of arenes with non-actived N-nucleophiles has been developed using sequential iron and copper catalysis. Regioselective ortho-activation of anisoles, anilines and phenols was achieved through iron(iii) triflimide catalysed iodination, followed by a copper(i)-catalysed, ligand-assisted coupling reaction with N-heterocycle, amide and sulfonamide-based nucleophiles. The synthetic utility of this one-pot, two-step method for the direct amination of ortho-aryl C-H bonds was demonstrated with the late-stage functionalisation of 3,4-dihydroquinolin-2-ones. This allowed the preparation of a TRIM24 bromodomain inhibitor and a series of novel analogues.

Dynamic stereochemistry transfer in a transannular aldol reaction: Total synthesis of hypocrellin A

(Chemical Equation Presented) A dynamic approach: The key step in the total synthesis of hypocrellin A involves a potentially biomimetic 1,8-diketone aldol reaction, which constructs the seven-membered ring. The helical configuration is established first

On the Synthesis of Tiliacora Alkaloids, II: Synthesis of the Asymmetrical Biphenyl Derivative

The biphenyl derivatives S-1 and S-3 were obtained by mixed Ullmann reaction of the phenylacetic esters 3, 4 and 5.Because they contain selectively removable protective groups for the carboxyl functions, S-1 and S-3 are proper intermediates for the constitution selective reaction with the former described asymmetrical dibenzo-1,4-dioxin derivative K.