90794-29-9

Basic information

• Product Name: Ethyl 2-(2-iodophenyl)acetate
• Synonyms: Ethyl 2-(2-iodophenyl)acetate;ethyl (2-iodophenyl)acetate
• CAS NO: 90794-29-9
• Molecular Formula: C₁₀H₁₁IO₂
• Molecular Weight: 290.09761
• Mol File: 90794-29-9.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: Ethyl 2-(2-iodophenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2-(2-iodophenyl)acetate(90794-29-9)
• EPA Substance Registry System: Ethyl 2-(2-iodophenyl)acetate(90794-29-9)

Safety Data

• Hazardous Substances Data: 90794-29-9(Hazardous Substances Data)

Usage

General Description

Ethyl 2-(2-iodophenyl)acetate is a chemical compound with the molecular formula C10H11IO2. It is commonly used in organic synthesis and pharmaceutical research as a key intermediate for the production of various compounds. Ethyl 2-(2-iodophenyl)acetate is usually prepared by the esterification of 2-(2-iodophenyl)acetic acid with ethanol, and it is known for its characteristic sweet and fruity odor. Ethyl 2-(2-iodophenyl)acetate is also used as a fragrance ingredient in perfumes and personal care products due to its pleasant aroma. Additionally, it is utilized in the production of flavors and fragrances, as well as in chemical research and development.

Upstream product

• 40400-13-3 2-Iodobenzyl bromide 
• 615-37-2 ortho-methylphenyl iodide 
• 64-17-5 ethanol 
• 18698-96-9 o-iodophenylacetic acid 
• 40400-15-5 2-(2-iodophenyl)acetonitrile 

Downstream Products

• 1417512-55-0 ethyl 2-(2-phenoxyphenyl)acetate 
• 154502-70-2 ethyl 2-(2-benzoylphenyl)acetate 
• 1178576-56-1 C₁₂H₁₁NO₂ 
• 1178576-57-2 (R)-3-methyl-5-oxo-2,3-dihydro-5H-oxazolo[3,2-b]isoquinoline-10-carboxylic acid ethyl ester 
• 1178576-55-0 C₁₅H₁₇NO₅ 
• 1178576-66-3 3-methyl-9-oxo-1-phenyl-1,2,3,9-tetrahydro-pyrazolo[1,5-b]isoquinoline-4-carboxylic acid ethyl ester 
• 1178576-65-2 9-oxo-1-phenyl-1,2,3,9-tetrahydro-pyrazolo[1,5-b]isoquinoline-4-carboxylic acid ethyl ester 
• 67213-70-1 2,3-dihydro-5H-oxazolo<3,2-b>isoquinolin-5-one 
• 1178576-49-2 C₁₄H₁₅NO₅ 
• 1095548-87-0 ethyl 2-(2-(3-(benzyloxy)prop-1-ynyl)phenyl)acetate 
• 1095548-81-4 ethyl 2-((2-(naphthalen-2-yl)ethynyl)phenyl)acetate 
• 1095548-84-7 ethyl 2-(2-((3-methoxyphenyl)ethynyl)phenyl)acetate 
• 1075683-89-4 ethyl 5-oxo-1,2,3,5-tetrahydropyrrolo[1,2-b]isoquinoline-10-carboxylate 
• 1075684-07-9 C₁₅H₁₇NO₄ 

Relevant articles and documents

One-Pot Base-Mediated Synthesis of Functionalized Aza-Fused Polycyclic Quinoline Derivatives

A new one-pot protocol has been developed for the facile and efficient synthesis of aza-fused polycyclic quinolines (e.g., pyrrolo[1,2-a]quinolines) by the base-catalyzed reaction of 2-formylpyrroles and 2-halophenylacetonitriles. This reaction proceeded under transition metal-free conditions and showed high functional group tolerance, with the desired products being formed in good yields.

Synthesis of indene derivatives via electrophilic cyclization

3-Iodo-1H-indene derivatives are synthesized by iodonium-promoted 5-endo-dig carbocyclization of 2-substituted ethynylmalonates. Various 2-substituted ethynylmalonates bearing aryl-, alkyl-and ether-protected propargyl alcohols were successfully converted

Palladium-catalyzed carboxamidation reaction and aldol condensation reaction cascade: A facile approach to ring-fused isoquinolinones

(Chemical Equation Presented) Palladium-catalyzed carboxamidation reaction and aldol condensation reaction cascade are very useful for the synthesis of various ABC ring substituted fused isoquinolinones.