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

Description

3,5-DIIODOTOLUENE, with the molecular formula C7H6I2, is a colorless to pale yellow liquid chemical compound derived from toluene. It features two iodine atoms attached to the benzene ring, making it a versatile reagent in organic synthesis. Despite its utility, it is classified as a hazardous substance that requires careful handling to prevent skin, eye, and respiratory system irritation or damage.

Uses

Used in Organic Synthesis:
3,5-DIIODOTOLUENE is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3,5-DIIODOTOLUENE is utilized as a key intermediate in the synthesis of certain drugs, playing a crucial role in the development of new medications.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 3,5-DIIODOTOLUENE serves as an intermediate in the production of various agrochemicals, aiding in the creation of substances that protect crops and enhance agricultural productivity.

Upstream product

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

Downstream Products

• 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 
• 1246452-34-5 C₁₄H₁₉I₂NO₃ 

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)