116632-41-8

Basic information

• Product Name: 2-CHLORO-5-IODOTOLUENE
• Synonyms: 2-CHLORO-5-IODOTOLUENE;2-CHLORO-5-IODOTOLUE;1-Chloro-4-iodo-2-methylbenzene;Benzene, 1-chloro-4-iodo-2-Methyl-
• CAS NO: 116632-41-8
• Molecular Formula: C₇H₆ClI
• Molecular Weight: 252.48
• Product Categories: Halogen toluene;Chlorine Compounds;Iodine Compounds;Aryl;C7;Halogenated Hydrocarbons;Building Blocks;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks
• Mol File: 116632-41-8.mol
• Article Data: 2

Chemical Properties

• Melting Point: 10 °C
• Boiling Point: 239 °C(lit.)
• Flash Point: 230 °F
• Appearance: Colorless to yellow/Liquid
• Density: 1.81 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.053mmHg at 25°C
• Refractive Index: n20/D 1.624(lit.)
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 2-CHLORO-5-IODOTOLUENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-5-IODOTOLUENE(116632-41-8)
• EPA Substance Registry System: 2-CHLORO-5-IODOTOLUENE(116632-41-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 116632-41-8(Hazardous Substances Data)

Usage

Uses

2-Chloro-5-iodotoluene may be used to synthesize:1-(4-chloro-3-methylphenyl)-1H-pyrrolo[2,3-c]pyridinebromomethyl-2-chloro-5-iodobenzene3-(4′-chloro-3′-tolyl)thiophene

General Description

2-Chloro-5-iodotoluene is a halogenated hydrocarbon.

InChI:InChI=1/C7H6ClI/c1-5-4-6(9)2-3-7(5)8/h2-4H,1H3

Upstream product

• 13290-74-9 1-chloro-2-methyl-4-nitrobenzene 
• 95-49-8 2-methylchlorobenzene 
• 7664-93-9 sulfuric acid 
• 7553-56-2 iodine 
• 64-19-7 acetic acid 
• 7697-37-2 nitric acid 
• 7149-75-9 3-methyl-4-chloroaniline 

Downstream Products

• 1425047-30-8 3-(4′-chloro-3′-tolyl)thiophene 
• 1067197-12-9 methyl N-[[2-chloro-5-[1-(4-methylphenyl)methyl-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate 
• 1067197-09-4 methyl N-[[2-chloro-5-[2-(4-methylphenyl)methyl-2H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate 
• 1067197-10-7 methyl N-[[2-chloro-5-[2-(4-chlorophenyl)-2H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate 
• 1067197-11-8 methyl N-[[2-chloro-5-[1-(4-chlorophenyl)-1H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate 
• 1067197-08-3 methyl N-[[2-chloro-5-(1H-1,2,3-triazol-5-yl)phenyl]methyl]carbamate 
• 251084-97-6 methyl N-[[2-chloro-5-ethynylphenyl]methyl]carbamate 
• 251085-25-3 methyl N-[[2-chloro-5-[2-(trimethylsilyl)ethynyl]phenyl]methyl]carbamate 
• 1067197-20-9 methyl [(2-chloro-5-iodophenyl)methyl]carbamate 
• 1375086-49-9 2-(4-Chloro-3-methylphenyl)malononitrile 
• 1375086-51-3 3-(4-Chloro-3-methylphenyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidin-2-amine 
• 1375087-50-5 N-[3-(4-chloro-3-methylphenyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidin-2-yl]-2-(cyclopentyloxy)acetamide 
• 1375087-25-4 N-[3-(4-chloro-3-methylphenyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidin-2-yl]-3-cyclopropylpropanamide 
• 1375086-48-8 N-[3-(4-chloro-3-methylphenyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidin-2-yl]-3-phenylpropanamide 

Relevant articles and documents

METHOD OF PRODUCING IODIZING AGENT, AND METHOD OF PRODUCING AROMATIC IODINE COMPOUND

A method of the present invention, for producing an iodizing agent, includes the step of electrolyzing iodine molecules in a solution by using an acid as a supporting electrolyte. This realizes (i) a method of producing an iodine cation suitable for use as an iodizing agent that does not require a sophisticated separation operation after iodizing reaction is completed, and (ii) an electrolyte used in the method. Further, a method of the present invention, for producing an aromatic iodine compound, includes the step of causing an iodizing agent, and an aromatic compound whose nucleus has one or more substituent groups and two or more hydrogen atoms, to react with each other under the presence of a certain ether compound. This realizes such a method of producing an aromatic iodine compound that position selectivity in iodizing reaction of an aromatic compound is improved.