49617-79-0

Basic information

• Product Name: 3,5-DIIODOTOLUENE
• Synonyms: 3,5-DIIODOTOLUENE
• CAS NO: 49617-79-0
• Molecular Formula: C₇H₆I₂
• Molecular Weight: 343.93
• Mol File: 49617-79-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 3,5-DIIODOTOLUENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIIODOTOLUENE(49617-79-0)
• EPA Substance Registry System: 3,5-DIIODOTOLUENE(49617-79-0)

Safety Data

• Hazardous Substances Data: 49617-79-0(Hazardous Substances Data)

Usage

General Description

3,5-DIIODOTOLUENE is a chemical compound with the molecular formula C7H6I2. It is a colorless to pale yellow liquid that is primarily used as a reagent in organic synthesis. It is derived from toluene and contains two iodine atoms attached to the benzene ring. The compound has been studied for its potential use in the production of pharmaceuticals and agrochemicals. However, it is important to handle 3,5-DIIODOTOLUENE with caution as it is considered a hazardous substance and exposure to high levels can cause irritation and damage to the skin, eyes, and respiratory system.

Upstream product

• 106-49-0 p-toluidine 
• 89677-87-2 1,2,3-triiodo-5-methylbenzene 
• 64662-57-3 2,6-diiodo-4-methylaniline 

Downstream Products

• 220117-56-6 3,5-Bis-{2-[2-propyloxy-5-(tetrahydro-2H-pyran-2-yloxy)-4-(2-triisopropylsilylethynyl)phenyl]ethynyl}toluene 
• 1169801-95-9 C₁₅H₁₆N₄ 
• 1073339-01-1 2-(3-iodo-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 120511-72-0 3,5-bis(2-cyanoprop-2-yl)toluene 
• 686351-25-7 1-(cyclopentylsulfonyl)-3-iodo-5-methylbenzene 
• 1446307-28-3 N-(3,5-diiodobenzyl)-2-[1,3-dimethylindol-2-ylmethylidene]-3-isopropylidenesuccinimide 
• 1446307-29-4 N-(3,5-diiodobenzyl)phthalimide 
• 1383916-53-7 1,3-bis(1,1-dimethylethyl) 2-(3-iodo-5-methylphenyl)propanedioate 
• 1384088-86-1 3-(4'-cyano-5,2'-dimethyl[1,1'-biphenyl]-3-yl)-2-hydroxy-4-oxo-1-(5-pyrimidinylmethyl)-4H-pyrido[1,2-a]pyrimidinium inner salt 
• 1246452-33-4 C₉H₁₁I₂NO 
• 1246452-39-0 C₅₈H₅₃NO₃ 
• 1246452-36-7 C₄₂H₄₅NO₃ 
• 1246452-38-9 C₇₆H₉₃NO₃Si₂ 
• 1246452-35-6 C₆₀H₈₅NO₃Si₂ 

Relevant articles and documents

Tuning the basicity of synergic bimetallic reagents: Switching the regioselectivity of the direct dimetalation of toluene from 2,5- to 3,5-positions

(Chemical Equation Presented) Meta-meta metalation: Remarkably, toluene can be directly dimanganated or dimagnesiated at the 3,5-positions using bimetallic bases with active Me3SiCH2 ligands (see scheme, blue). In contrast, n-butyl l

An all-photonic molecule-based parity generator/checker for error detection in data transmission

The function of a parity generator/checker, which is an essential operation for detecting errors in data transmission, has been realized with multiphotochromic switches by taking advantage of a neuron-like fluorescence response and reversible light-induced transformations between the implicated isomers.

Synthesis and magnetic behaviour of polyradical: Poly(1,3-phenyleneethynylene) with π-toporegulated pendant stable aminoxyl and imine N-oxide-aminoxyl radicals

The palladium-catalysed polycondensation of N-tert-butyl-N-(3,5-diethynylphenyl)aminoxyl with 2-(3,5-diiodophenyl)-4,4,5,5-tetramethyl-3-oxido-2-imidazolin-3-ium-l-yloxyl in pyridine-triethylamine at room temperature afforded poly(l,3-phenyleneethynylene)