936098-39-4

Basic information

• Product Name: methyl (4-chloro-2-iodophenyl)acetate
• Synonyms: methyl (4-chloro-2-iodophenyl)acetate
• CAS NO: 936098-39-4
• Molecular Weight: 310.519
• Mol File: 936098-39-4.mol

Chemical Properties

• CAS DataBase Reference: methyl (4-chloro-2-iodophenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (4-chloro-2-iodophenyl)acetate(936098-39-4)
• EPA Substance Registry System: methyl (4-chloro-2-iodophenyl)acetate(936098-39-4)

Safety Data

• Hazardous Substances Data: 936098-39-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Methyl (4-chloro-2-iodophenyl)acetate is used as an intermediate in the synthesis of aldosterone synthase inhibitors for the treatment of hypertension and other cardiovascular diseases. Its role in the synthesis process contributes to the development of effective medications that help regulate aldosterone levels in the body, thus managing blood pressure and preventing related complications.

Upstream product

• 13421-13-1 4-chloro-2-iodobenzoic acid 
• 882689-31-8 2-(4-chloro-2-iodophenyl)acetonitrile 
• 882689-32-9 4-chloro-1-(chloromethyl)-2-iodobenzene 
• 244104-55-0 (4-chloro-2-iodophenyl)methanol 
• 67-56-1 methanol 
• 936098-38-3 2-(4-chloro-2-iodophenyl)acetic acid 

Downstream Products

• 936098-40-7 methyl (4-chloro-2-vinylphenyl)acetate 
• 22482-73-1 5-chloro-2-(2-methoxy-2-oxoethyl)benzoic acid 
• 936098-52-1 [4-chloro-2-({(3S)-4-[ (4-chlorophenyl)acetyl]-3-methylpiperazin-1-yl}methyl) phenyl]acetic acid 
• 936098-44-1 methyl [4-chloro-2-(hydroxymethyl)phenyl]acetate 
• 1159358-87-8 [4-chloro-2-({(3S)-4-[ (4-chlorophenyl)acetyl]-3-methylpiperazin-1-yl}methyl) phenyl]acetic acid methyl ester 

Relevant articles and documents

Zwitterionic CRTh2 antagonists

A novel series of zwitterions is reported that contains potent, selective antagonists of the chemoattractant receptor-homologous expressed on Th2 lymphocytes receptor (CRTh2 or DP2). A high quality lead compound 2 was discovered from virtual screening based on the pharmacophore features present in a literature compound 1. Lead optimization through side chain modification and preliminary changes around the acid are disclosed. Optimization of physicochemical properties (log D, MWt, and HBA) allowed maintenance of high CRTh2 potency while achieving low rates of metabolism and minimization of other potential concerns such as hERG channel activity and permeability. A step-change increase in potency was achieved through addition of a single methyl group onto the piperazine ring, which gave high quality compounds suitable for progression into in vivo studies.

Novel Compounds

The invention relates to substituted aryl acids as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.