38954-00-6

Basic information

• Product Name: Benzene, 1-(2-iodoethyl)-4-methoxy-
• Synonyms: 4-(2-iodo-ethyl)-anisole;4-(2-Jod-aethyl)-anisol;2-(4-methoxyphenyl)ethyl iodide;1-(2-iodoethyl)-4-methoxybenzene;4-methoxyphenethyl iodide;1-(2-Iodo-ethyl)-4-methoxy-benzene
• CAS NO: 38954-00-6
• Molecular Formula: C9H11IO
• Molecular Weight: 262.09
• Mol File: 38954-00-6.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 117 - 119 °C (1 mmHg)
• CAS DataBase Reference: Benzene, 1-(2-iodoethyl)-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(2-iodoethyl)-4-methoxy-(38954-00-6)
• EPA Substance Registry System: Benzene, 1-(2-iodoethyl)-4-methoxy-(38954-00-6)

Safety Data

• Hazardous Substances Data: 38954-00-6(Hazardous Substances Data)

Upstream product

• 5107-52-8 2-(p-methoxyphenyl)ethyl toluene-p-sulphonate 
• 702-23-8 2-(4-Methoxyphenyl)ethanol 
• 141666-87-7 1-Tosyl-1-<2-(4-methoxyphenyl)ethyl>hydrazine 
• 1929-29-9 3-(4-methoxyphenyl)propanoic acid 
• 23786-14-3 4-methoxy-phenyl acetic acid methyl ester 
• 18217-00-0 1-(2-Chloroethyl)-4-methoxybenzene 
• 141666-92-4 4-methyl-N-[2-(4-methoxyphenyl)ethyl]benzenesulfonamide 
• 104-01-8 4-Methoxyphenylacetic acid 

Downstream Products

• 208400-76-4 3-ethoxy-6-[2-(4-methoxy-phenyl)-ethyl]-cyclohex-2-enone 
• 51125-16-7 5-(4-methoxyphenyl)-1-pentene 
• 1027664-82-9 dimethyl [2-(4-methoxyphenyl)ethyl]malonate 

Relevant articles and documents

Electrophilic Cyanative Alkenylation of Arenes

A variety of appropriately substituted internal alkynes were transformed into the corresponding cyano-substituted phenanthrenes, dihydronaphthalenes, and cyclohepta-1,3,5-trienes in moderate to excellent yields by treatment with imidazolium thiocyanate 1, which serves as an easy to handle [CN]+ precursor, in the presence of BCl3. The synthetic value of the method is additionally demonstrated by the transformation of the primarily obtained products into heavily substituted quinolines. Additionally, the dynamic properties of the prepared dibenzocyclohepta-1,3,5-trienes have been investigated.

Direct Access to Isotopically Labeled Aliphatic Ketones Mediated by Nickel(I) Activation

An extensive range of functionalized aliphatic ketones with good functional-group tolerance has been prepared by a NiI-promoted coupling of either primary or secondary alkyl iodides with NN2 pincer NiII-acyl complexes. The latter were easily accessed from the corresponding NiII-alkyl complexes with stoichiometric CO. This Ni-mediated carbonylative coupling is adaptable to late-stage carbon isotope labeling, as illustrated by the preparation of isotopically labelled pharmaceuticals. Preliminary investigations suggest the intermediacy of carbon-centered radicals.

Transition-Metal-Free Borylation of Alkyl Iodides via a Radical Mechanism

We describe an operationally simple transition-metal-free borylation of alkyl iodides. This method uses commercially available diboron reagents as the boron source and exhibits excellent functional group compatibility. Furthermore, a diverse range of prim