49617-79-0

Usage

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

• 89677-87-2 1,2,3-triiodo-5-methylbenzene 
• 106-49-0 p-toluidine 
• 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 
• 350589-29-6 3,5-bis-{2-[2,5-dipropyloxy-4-(2-triisopropylsilylethynyl)phenyl]ethynyl}toluene 
• 686351-24-6 1-(cyclopentylthio)-3-iodo-5-methylbenzene 
• 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 

Relevant academic research and scientific papers

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

NEW COMPOUND

PROBLEM TO BE SOLVED: To provide a new compound that does not have structural similarity to ceramide and has excellent CERT inhibitory activity. SOLUTION: The present invention provides a new compound of structural formula (I). A bond group -X- is cis-cyclopropyl-, R1, R2, R3, R4, and R5 independently represent a hydrogen atom, a halogen atom, a linear or branched C1-C8 alkyl group that may have a halogen atom, or OR6. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2020,JPOandINPIT

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.

A mild and convenient synthesis of 1,2,3-triiodoarenes via consecutive iodination/diazotization/iodination strategy

A mild and convenient synthesis of 1,2,3-triiodoarenes has been developed. This method consists of two steps which can be performed on multigram scale with moderate to excellent yields. This report discloses a practical synthesis of 1,2,3-triiodoarenes and 1,2,3-trihaloarenes that is general in scope, operationally simple, scalable, and is easy to workup and to purify. We also report the first regioselective transmetalation reaction of 1,2,3-triiodoarenes to provide ortho-diiodoaryl derivatives, which are useful building blocks and indeed are hard to make by other means. CSIRO 2013.

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)