19099-56-0

Basic information

• Product Name: 3-Iodoisopropylbenzene
• Synonyms: 1-Iodo-3-isopropylbenzene; Benzene, 1-iodo-3-(1-methylethyl)-
• CAS NO: 19099-56-0
• Molecular Formula: C₉H₁₁I
• Molecular Weight: 246
• Mol File: 19099-56-0.mol

Chemical Properties

• Boiling Point: 231.6°C at 760 mmHg
• Flash Point: 100.2°C
• Appearance: /
• Density: 1.523g/cm³
• Vapor Pressure: 0.0939mmHg at 25°C
• Refractive Index: 1.574
• CAS DataBase Reference: 3-Iodoisopropylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Iodoisopropylbenzene(19099-56-0)
• EPA Substance Registry System: 3-Iodoisopropylbenzene(19099-56-0)

Safety Data

• Hazardous Substances Data: 19099-56-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
3-Iodoisopropylbenzene is used as a reagent in organic synthesis for its ability to participate in nucleophilic substitution and other synthetic pathways. Its unique structure allows it to be a versatile building block in the creation of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3-Iodoisopropylbenzene is used as a key intermediate in the synthesis of various pharmaceuticals. Its role in the production process is to provide a starting material or a building block for the development of new drugs and medicinal compounds.
Used in Agrochemical Production:
3-Iodoisopropylbenzene also finds application in the agrochemical sector, where it is used in the synthesis of agrochemicals. It serves as a precursor in the production of pesticides, herbicides, and other agricultural chemicals, contributing to the development of effective solutions for crop protection.
Used in the Production of Fine Chemicals:
In the fine chemicals industry, 3-Iodoisopropylbenzene is employed as a building block for the synthesis of specialty chemicals. Its unique properties make it suitable for the production of high-value chemicals used in various applications, such as fragrances, dyes, and other specialty products.

InChI:InChI=1/C9H11I/c1-7(2)8-4-3-5-9(10)6-8/h3-7H,1-2H3

Upstream product

• 5369-16-4 meta-iso-propyl aniline 

Downstream Products

• 645389-03-3 2-(3-isopropylphenyl)-6-methoxy-3,4-dihydroisoquinolin-1(2H)-one 
• 645394-30-5 4-[2-(3-isopropyl-phenyl)-6-methoxy-1-methyl-1,2,3,4-tetrahydro-isoquinolin-1-yl]-phenol 
• 645393-12-0 1-(4-benzyloxy-phenyl)-2-(3-isopropyl-phenyl)-6-methoxy-1-methyl-1,2,3,4-tetrahydro-isoquinoline 
• 645399-23-1 2-(3-isopropyl-phenyl)-6-methoxy-1-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-1,2,3,4-tetrahydro-isoquinoline 
• 179063-40-2 N,N'-bis(3-methylphenyl)-N,N'-bis(3-isopropylphenyl)-2,3-naphthylenediamine 
• 817624-72-9 methyl 3-isopropylcinnamate 

Relevant articles and documents

Synthesis of Azepino[1,2-a]indole-10-amines via [6+1] Annulation of Ynenitriles with Reformatsky Reagent

Lewis acid-catalyzed [6+1] annulation reactions of 2-cyano-1-propargyl- and 2-alkynyl-1-cyanomethyl-indoles with Reformatsky reagent are described. 8-Aryl, 8-alkyl-, 8-hetaryl-, 9-aryl, and 9-alkyl-azepino[1,2-a]indole amines were obtained through a 7-endo-mode cyclization of the β-aminoacrylate intermediates. The antiproliferative activity of the azepino[1,2-a]indoles analogs against the HCT-116 cells were also examined.