73029-52-4

Usage

Uses

Used in Organic Synthesis:
(2-IODO-5-METHOXYPHENYL)ACETIC ACID is used as a building block for the synthesis of more complex organic molecules. Its unique structure and functional groups allow for the creation of a wide range of compounds with diverse properties and potential applications.
Used in Pharmaceutical Research:
(2-IODO-5-METHOXYPHENYL)ACETIC ACID is used as a starting material for the development of new drugs and materials. Its potential pharmacological properties are currently being investigated, and ongoing research may lead to the discovery of new therapeutic agents and applications in the medical field.
Used in Chemical Research:
(2-IODO-5-METHOXYPHENYL)ACETIC ACID is used as a research tool in the study of chemical reactions and mechanisms. Its unique structure and functional groups provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.
Used in Material Science:
(2-IODO-5-METHOXYPHENYL)ACETIC ACID has potential applications in the development of new materials with specific properties. Its unique structure and functional groups may be utilized to create materials with improved performance characteristics, such as enhanced stability, reactivity, or selectivity.

Upstream product

• 1798-09-0 m-methoxyphenylacetic acid 

Downstream Products

• 54413-97-7 <5-methoxy-2-(4-methylthiophenylthio)phenyl>acetic acid 
• 2503-24-4 5-methoxybenzofuran-2(3H)-one 
• 92424-06-1 bis[4-(methanesulfonyl)phenyl] disulfide 
• 98190-65-9 <5-Methoxy-2-(4-methylsulfonylphenylthio)phenyl>acetic Acid 
• 112399-38-9 (2-Iodo-5-methoxy-phenyl)-acetyl chloride 
• 73038-88-7 [5-Methoxy-2-(4-methoxy-phenylsulfanyl)-phenyl]-acetic acid 
• 99540-20-2 (6-iodo-3-methoxy)phenyl-N,N-dimethylacetamide 
• 1301714-65-7 N-butyl-2-(2-ethynyl-5-methoxyphenyl)acetamide 
• 1301714-79-3 N-butyl-2-(2-(2-(butylamino)-2-oxoethyl)-4-methoxyphenyl)-7-methoxy-4-methyl-1-naphthamide 
• 1610054-80-2 (R)-3-(2-iodo-5-methoxyphenyl)oxetan-2-one 
• 1610054-61-9 methyl 2-diazo-2-(2-chloro-5-methoxyphenyl)acetate 
• 99540-02-0 5-methoxy-N,N-dimethyl-2-(phenylethynyl)benzeneethanamine 
• 99540-37-1 2-iodo-5-methoxy-N,N-dimethylbenzeneethanamine 
• 888030-01-1 N-Boc-N-nosyl-2-(4-(2-(2-aminoethyl)-4-methoxyphenyl)-1-methoxycyclohex-3-enyl)ethanol 

Relevant academic research and scientific papers

Synthesis of Substituted Benzo[ b]thiophenes via Base-Promoted Domino Condensation-Intramolecular C-S Bond Formation

A novel synthesis of 2,3-substituted benzothiophenes is reported, involving a tandem base-mediated condensation of o-iodoarylacetonitriles/acetates/ketones with (hetero)aryldithioesters and an intramolecular C-S bond formation. The reaction affords divers

Synthesis of N-Glycosyl-2-oxindoles by Pd-Catalyzed N-Arylation of 1-Amidosugars

An efficient intramolecular Pd-catalyzed N-arylation of o-iodo-amidosugars for the synthesis of N-glycosylated oxindoles has been reported. The coupling reaction takes place in toluene and involves Pd(OAc)2/RuPhos catalytic systems in the presence of K2CO3. This versatile approach was extended successfully to the synthesis of other N-glycosylated heterocycles.

Efficient synthesis of heterocyle-fused β-naphthylamines via intramolecular addition to a cyano group initiated by nucleopalladation of alkynes

A palladium(II)-catalyzed efficient synthesis of heterocycle-fused-naphthylamines was accomplished via nucleophilic addition of a carbon-palladium bond to the intramolecular cyano group initiated by nucleopalladation (oxypalladation or aminopalladation) o

Methods for the treatment of hypertension

Acetylene compounds of the formula (I): STR1 wherein Y, R1, R2, R3, and R4 are as described herein, m is 0-3, n is 0-2 and Ar is phenyl or an aromatic heterocycle are disclosed. The compounds possess antihyperte

Acetylene amines and their use as vasodilators and antihypertensives

Acetylenes of the following formula (I): STR1 wherein Y, m, R1, R2, R3, n and R4 are defined herein and R5 is hydrogen, alkyl, cycloalkyl or substituted alkyl are useful vasodilators and antihypertens

Aralykyl (arylethynyl)aralkyl amines and their use as vasodilators and antihypertensives

Acetylenes of the formula (I): STR1 wherein Y, m, R1, R2 q, Alk, R3, n and R4 are as defined herein and Ar1 and Ar2 are aromatic, including the salts and ammonium derivatives of formula (I), in treating angina, hypertension and cardiac arrhythmias. Pharmaceutical compositions, methods of use and synthesis and novel intermediates are also part of the invention.