113379-13-8

Basic information

• Product Name: Benzene, 1-(3-iodopropyl)-4-methoxy-
• Synonyms: 3-(p-methoxyphenyl)-1-iodopropane;3-(4-Methoxyphenyl)-propyl iodide;3-(4-methoxyphenyl)propyl iodide;3-(4-methoxyphenyl)propyliodide
• CAS NO: 113379-13-8
• Molecular Formula: C10H13IO
• Molecular Weight: 276.117
• Mol File: 113379-13-8.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 293.9±23.0 °C(Predicted)
• Density: 1.520±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzene, 1-(3-iodopropyl)-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(3-iodopropyl)-4-methoxy-(113379-13-8)
• EPA Substance Registry System: Benzene, 1-(3-iodopropyl)-4-methoxy-(113379-13-8)

Safety Data

• Hazardous Substances Data: 113379-13-8(Hazardous Substances Data)

Upstream product

• 179548-39-1 4-(3-iodopropyl)phenol 
• 74-88-4 methyl iodide 
• 50893-53-3 carbonochloridic acid 1-chloro-ethyl ester 
• 5406-18-8 3-(p-methoxyphenyl)-1-propanol 
• 1963-36-6 4-methoxycinnamaldehyde 
• 72456-64-5 1-methanesulfonyloxy-3-(4-methoxyphenyl)propane 

Downstream Products

• 351388-30-2 (2R,3R,R_S)-(-)-2-[3-(4-methoxyphenyl)propyl]-2-(p-tolylsulfinyl)-1,3-diphenylaziridine 
• 351388-29-9 (1R,2R,R_S)-(-)-2-chloro-5-(4-methoxyphenyl)-1-phenyl-1-(phenylamino)-2-(p-tolylsulfinyl)pentane 
• 351388-31-3 (2S,3R)-(-)-2-decyl-2-[3-(4-methoxyphenyl)propyl]-1,3-diphenylaziridine 

Relevant articles and documents

Triphenylphosphine-Catalyzed Alkylative Iododecarboxylation with Lithium Iodide under Visible Light

Under irradiation of 456 nm blue light-emitting diodes, PPh3 catalyzes the iododecarboxylation of aliphatic carboxylic acid derived N-(acyloxy)phthalimide with lithium iodide as an iodine source. The reaction delivers primary, secondary, and bridgehead te

Introduction of Cyclopropyl and Cyclobutyl Ring on Alkyl Iodides through Cobalt-Catalyzed Cross-Coupling

A cobalt-catalyzed cross-coupling between alkyl iodides and cyclopropyl, cyclobutyl, and alkenyl Grignard reagents is disclosed. The reaction allows the introduction of strained rings on a large panel of primary and secondary alkyl iodides. The catalytic system is simple and nonexpensive, and the reaction is general, chemoselective, and diastereoconvergent. The alkene resulting from the cross-coupling can be transformed to substituted cyclopropanes using a Simmons-Smith reaction. The formation of radical intermediates during the coupling is hypothesized.

Nickel-Catalyzed C-Alkylation of Nitroalkanes with Unactivated Alkyl Iodides

Enabled by nickel catalysis, a mild and general catalytic method for C-alkylation of nitroalkanes with unactivated alkyl iodides is described. Compatible with primary, secondary, and tertiary alkyl iodides; and tolerant of a wide range of functional groups, this method allows rapid access to diverse nitroalkanes.