29527-87-5

Basic information

• Product Name: (2-Iodopropyl)benzene
• Synonyms: (2-Iodopropyl)benzene;2-Iodo-1-phenylpropane
• CAS NO: 29527-87-5
• Molecular Formula: C₉H₁₁I
• Molecular Weight: 246.08811
• Mol File: 29527-87-5.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2-Iodopropyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (2-Iodopropyl)benzene(29527-87-5)
• EPA Substance Registry System: (2-Iodopropyl)benzene(29527-87-5)

Safety Data

• Hazardous Substances Data: 29527-87-5(Hazardous Substances Data)

Usage

General Description

(2-Iodopropyl)benzene, also known as 1-(2-iodopropyl)benzene, is a chemical compound with the molecular formula C9H11I. It is a halogenated alkylbenzene with a 2-iodopropyl substituent attached to the benzene ring. This chemical is commonly used as an intermediate in organic synthesis to create various pharmaceuticals, agrochemicals, and other fine chemicals. It is also used in the production of flavors and fragrances. The compound is known to have some toxicity and should be handled with care, following proper safety protocols.

Upstream product

• 4362-18-9 2-benzyl-2-methyl-1,3-dioxolane 
• 1009-67-2 2-methyl-3-phenylpropanoic acid 
• 300-57-2 allylbenzene 
• 103-79-7 1-phenyl-acetone 
• 5406-60-0 2-benzyl-2,4,5-trimethyl-1,3-dioxolan 
• 698-87-3 3-phenyl-2-propanol 
• 14135-71-8 1-phenyl-2-propyl-4-toluenesulfonate 

Downstream Products

• 17322-34-8 (2-nitropropyl)benzene 
• 80826-96-6 1-phenyl-2-propyl nitrite 
• 5814-85-7 1,2-diphenylpropane 
• 1604039-76-0 N,N-dimethyl-4-(3-methyl-4-phenylbut-1-yn-1-yl)aniline 
• 1604039-75-9 1-(tert-butyl)-4-(3-methyl-4-phenylbut-1-yn-1-yl)benzene 
• 1380434-39-8 1-(4-tert-butylphenyl)-2-methyl-3-phenylpropan-1-one 
• 4842-43-7 2-methyl-1,3-diphenylpropan-1-one 

Relevant articles and documents

Merging Halogen-Atom Transfer (XAT) and Copper Catalysis for the Modular Suzuki-Miyaura-Type Cross-Coupling of Alkyl Iodides and Organoborons

We report here a mechanistically distinct approach to achieve Suzuki-Miyaura-type cross-couplings between alkyl iodides and aryl organoborons. This process requires a copper catalyst but, in contrast with previous approaches based on palladium and nickel

Photochemical Decarboxylative C(sp3)-X Coupling Facilitated by Weak Interaction of N-Heterocyclic Carbene

While N-hydroxyphthalimide (NHPI) ester has emerged as a powerful reagent as an alkyl radical source for a variety of C-C bond formations, the corresponding C(sp3)-N bond formation is still in its infancy. We demonstrate herein transition-metal-free decarboxylative C(sp3)-X bond formation enabled by the photochemical activity of the NHPI ester-NaI-NHC complex, giving primary C(sp3)-(N)phth, secondary C(sp3)-I, or tertiary C(sp3)-(meta C)phth coupling products. The primary C(sp3)-(N)phth coupling offers convenient access to primary amines.

Method of preparing iodine alkane by using rhodium catalysis

The invention relates to the field of organic synthesis and discloses a synthetic method of iodine alkane. The synthetic method of the iodine alkane, disclosed by the invention, comprises the following steps: taking olefin as a starting raw material, adding a rhodium metal catalyst, a phosphine ligand, a solvent and molecular iodine into a pressurizing reaction kettle, introducing hydrogen and then synthesizing a series of the iodine alkane by using one-step reaction. The reaction temperature is 0 to 60 DEG C, the molar ratio of the rhodium metal to the olefin is (0.00001 to 1) to (0.1 to 1) and the molar ratio of the iodine to the olefin is (0.5 to 1) to (10 to 1). The synthetic method of the iodine alkane, disclosed by the invention, has obvious advantages of wide application range, short process flow and low cost of the raw materials; the synthetic method of the iodine alkane is suitable for industrialized production of a series of the iodine alkanes.