61926-37-2

Basic information

• Product Name: Benzene, 1-(iodoethynyl)-4-methoxy-
• Synonyms: 1-iodoethynyl-4-methoxybenzene;Benzene,1-(iodoethynyl)-4-methoxy;4-(iodoethynyl)anisole;(4-methoxyphenyl)ethynyl iodide
• CAS NO: 61926-37-2
• Molecular Formula: C9H7IO
• Molecular Weight: 258.058
• Mol File: 61926-37-2.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(iodoethynyl)-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(iodoethynyl)-4-methoxy-(61926-37-2)
• EPA Substance Registry System: Benzene, 1-(iodoethynyl)-4-methoxy-(61926-37-2)

Safety Data

• Hazardous Substances Data: 61926-37-2(Hazardous Substances Data)

Upstream product

• 768-60-5 4-methoxyphenylacetylen 
• 3989-14-8 (4-methoxyphenylethynyl)trimethylsilane 
• 2227-57-8 3-(4-methoxyphenyl)propynoic acid 
• 33675-41-1 1-bromo-2-(4-methoxyphenyl)acetylene 
• 1111758-19-0 1,1-diiodo-2-(4-methoxyphenyl)ethene 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 22779-05-1 1,4-bis(4-methoxyphenyl)-1,3-butadiyne 
• 151362-06-0 1,4-bis[4-(trifluoromethyl)phenyl]buta-1,3-diyne 
• 24785-38-4 1-methoxy-4-[2-(4-methylphenyl)ethynyl]benzene 
• 1403848-67-8 3-(1,3-bis(4-methoxyphenyl)prop-2-yn-1-yl)-1-methyl-1H-indole 
• 116557-81-4 1-benzyl-4-(4-methoxy)phenyl-1H-1,2,3-triazole 
• 768-60-5 4-methoxyphenylacetylen 
• 1198769-65-1 4-(4-methoxyphenyl)-5-phenyl-1-p-tolyl-1H-1,2,3-triazole 
• 18277-20-8 hexadeca-7,9-diyne 

Relevant articles and documents

Synthesis method of 1-iodo-alkyne compound

The invention discloses a synthetic method of a 1-iodo-alkyne compound. The preparation method comprises the following steps: in an aerobic environment, mixing terminal alkyne, soluble inorganic iodized salt, sodium phenylsulfinate or a derivative thereof

Au(I)-Catalyzed Hydration of 1-Iodoalkynes Leading to α-Iodoketones

A catalytic protocol for the Au(I)-catalyzed hydration of 1-iodoalkynes is disclosed. The use of Au(I)–NHC catalyst enabled the straightforward synthesis of a variety of α-iodomethyl ketones in good to excellent yields. The utility of this simple method is further highlighted by showcasing iodination/hydration and hydration/oxidation sequential protocols leading to the construction of molecular complexity.

Preparation method of 1-iodoalkyne

The invention discloses a preparation method of 1-iodoalkyne. The method comprises the following step: reacting a terminal alkyne compound with N-iodosuccinimide in a solvent in the presence of aluminum oxide and a molecular sieve to prepare a 1-iodoalkyn