4296-15-5

Basic information

• Product Name: 2-IODOETHYL METHYL ETHER
• Synonyms: 1-IODO-2-METHOXYETHANE;2-IODOETHYL METHYL ETHER;Ethane,1-iodo-2-methoxy- (9CI)
• CAS NO: 4296-15-5
• Molecular Formula: C₃H₇IO
• Molecular Weight: 185.99
• Mol File: 4296-15-5.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 134.4 °C at 760 mmHg
• Flash Point: 35.1 °C
• Appearance: /
• Density: 1.801 g/cm³
• Vapor Pressure: 10mmHg at 25°C
• Refractive Index: 1.505
• Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
• CAS DataBase Reference: 2-IODOETHYL METHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-IODOETHYL METHYL ETHER(4296-15-5)
• EPA Substance Registry System: 2-IODOETHYL METHYL ETHER(4296-15-5)

Safety Data

• Hazardous Substances Data: 4296-15-5(Hazardous Substances Data)

Usage

General Description

2-Iodoethyl methyl ether, also known as methyl 2-iodoethyl ether, is a chemical compound with the molecular formula C3H7IO. It is a colorless liquid with a strong, sweet odor, and is primarily used as a reagent in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. It is also used as a solvent in chemical reactions and as a coupling agent in the synthesis of certain chemical compounds. Due to its strong odor and potential health hazards, proper handling and ventilation are necessary when working with 2-iodoethyl methyl ether. Additionally, it is important to store and dispose of this compound in accordance with local regulations and safety guidelines.

InChI:InChI=1/C3H7IO/c1-5-3-2-4/h2-3H2,1H3

Upstream product

• 67-56-1 methanol 
• 26466-04-6 methyl hypoiodite 
• 74-85-1 ethene 
• 624-73-7 1,2-Diiodoethane 
• 17178-10-8 2-methoxy-ethyl p-toluenesulfonyloxy ester 
• 627-42-9 2-chloroethyl methyl ether 
• 67-64-1 acetone 
• 6482-24-2 2-Bromoethyl methyl ether 
• 762-51-6 1-fluoro-2-iodoethane 
• 75-21-8 oxirane 
• 74-88-4 methyl iodide 
• 106-93-4 ethylene dibromide 
• 109-86-4 2-methoxy-ethanol 

Downstream Products

• 227305-66-0 1-bromo-3-(2-methoxyethoxy)benzene 
• 74-88-4 methyl iodide 
• 104703-54-0 trisylhydrazone de la cyclopentenyl-2 (methoxy-2 ethyl)-2 cyclopentanone-1 
• 104703-46-0 tosylhydrazone de la cyclopentenyl-2 (methoxy-2 ethyl)-2 cyclopentanone-1 
• 142677-35-8 (+/-)-(1S*,2S*,5R*,6S*)-2-(2,6-Dimethoxyphenoxy)-1-hydroxy-6-<2-methoxy-5-(2-methoxyethoxy)phenyl>-3,7-dioxabicyclo<3.3.0>octane 
• 120505-07-9 7-(2,5-dioxahexyl)-7-methyl-2,5,9,12-tetraoxatridecane 
• 502-72-7 cyclopentadecanone 
• 77857-81-9 (R)-2-(2-methoxyethyl)cyclopentadecanone 
• 77857-81-9 (S)-(+)-2-(2-methoxyethyl)cyclopentadecanone 
• 830-13-7 cyclododecanone 
• 77857-83-1 (R)-2-(2-methoxyethyl)cyclododecanone 
• 77857-83-1 (S)-(+)-2-(2-methoxyethyl)cyclododecanone 
• 1502-06-3 cyclodecanone 
• 77857-84-2 (S)-2-(2-methoxyethyl)cyclodecanone 

Relevant articles and documents

-

-

-

-

SUBSTITUTED OXOPYRIDINE DERIVATIVES AND USE THEREOF IN THE TREATMENT OF CARDIOVASCULAR DISORDERS

The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

Synthesis of pyrrolidinium-based poly(ionic liquid) electrolytes with poly(ethylene glycol) side chains

The synthesis and characterization of a new family of pyrrolidinium based poly(ionic liquid) (PIL) electrolytes with poly(ethylene glycol) (PEG) pendant groups is reported. The PILs were synthesized from a diallyl methyl amine hydrochloride monomer, which