60070-06-6

Usage

Physical state

Colorless liquid at room temperature

Uses

a. Intermediate in the synthesis of various organic compounds
b. Building block in the production of pharmaceuticals, dyes, and polymers
c. Manufacture of agricultural chemicals
d. Reagent in organic chemistry
e. Cross-linking agent in the production of polymers and resins

Safety precautions

Can be harmful if ingested, inhaled, or makes contact with the skin; proper handling required

Upstream product

• 50-00-0 formaldehyd 
• 95-47-6 o-xylene 
• 69094-40-2 diethyl 4,5-dimethylphthalate 
• 2362-16-5 1,2-bis(chloromethyl)-4,5-dimethylbenzene 
• 60070-05-5 1,2-bis(hydroxymethyl)-4,5-dimethylbenzene 

Downstream Products

• 1373318-35-4 C₅₅H₄₂O 
• 1373318-36-5 C₈₇H₅₈O 
• 1373318-32-1 C₅₇H₄₆O₂ 
• 1556864-54-0 6,7-dimethyl-3-phenyl-2-naphthonitrile 
• 1556864-56-2 3-(4-bromophenyl)-6,7-dimethyl-2-naphthonitrile 
• 1556864-60-8 3-(3,4-dimethylphenyl)-6,7-dimethyl-2-naphthonitrile 
• 1556864-62-0 3-(3,4-dichlorophenyl)-6,7-dimethyl-2-naphthonitrile 
• 24006-87-9 4,5-dimethyl-1,2-bis-cyanomethyl-benzene 
• 1616788-09-0 5,6-dimethyl-2-(3-phenylprop-2-yn-1-yl)isoindoline 
• 1407188-06-0 3-(2-(bromomethyl)-4,5-dimethylbenzyl)-1-dodecyl-3-((3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)sulfonyl)-2-oxoindolin-6-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate 
• 27286-83-5 1,2-Bis-(1,2-dibromo-2-phenyl-ethyl)-4,5-dimethyl-benzene 
• 27409-94-5 Tetramethylverden 
• 27286-84-6 ((4,5-dimethyl-1,2-phenylene)bis(ethyne-2,1-diyl))dibenzene 
• 27286-82-4 1,2-Bis-phenylethenyl-4,5-dimethyl-benzol 

Relevant academic research and scientific papers

Arene Substitution Design for Controlled Conformational Changes of Dibenzocycloocta-1,5-dienes

We report that an agile eight-membered cycloalkane can be stabilized by fusing a benzene ring on each side, substituted with proper functional groups. The conformational change of dibenzocycloocta-1,5-diene (DBCOD), a rigid?flexible?rigid organic moiety,

Organic thin film transistors based on 2,3-dimethylpentacene and 2,3-dimethyltetracene

2,3-Dimethylpentacene (DMP) and 2,3-dimethyltetracene (DMT) were synthesized, characterized and employed as the channel material in the fabrication of thin-film transistors. The two methyl groups increase the chemical stability of the compounds versus the

Methyl and Dimethyl o-Xylenyl-Substituted Fullerene Acceptors for Polymer Solar Cells

A series of fullerene derivatives based on methyl- and dimethyl-substituted o-xylenyl groups were synthesized via Diels-Alder reaction from fullerene (C60) and dienes derived from α,α′-dibromo-o-xylene derivatives. The synthesized 1-methyl-4,5-

Closely stacked oligo(phenylene ethynylene)s: Effect of π-stacking on the electronic properties of conjugated chromophores

In this work, a bicyclo[4.4.1]undecane scaffold is used to hold oligo(phenylene ethynylene) units in a cofacially stacked arrangement along the entire length of the conjugated units. We study the impact that the resulting strong interchain interactions ha

Phase tag-assisted synthesis of benzo[ b ]carbazole end-capped oligothiophenes

The introduction and removal of a phase tag have been used to trigger cyclization events in a new synthesis of benzo[b]carbazoles. The approach has been exploited in a tag-assisted approach to new benzo[b]carbazole end-capped oligothiophenes for prelimina

Fullerene Derivatives and Organic Electronic Device Comprising the Same

The present invention relates to fullerene derivatives and an organic electronic device using the same, and more specifically, to a novel fullerene derivative incorporating an aromatic fused ring compound and to an organic electronic device with excellent

Regioselective bromomethylation of 1,2-dialkylbenzenes

This paper describes a systematic exploration of the regioselective bromomethylation of 1,2-dialkylbenzenes as a function of the reaction temperature and the chain length of the alkyl groups. At both 80 and 110 °C, bromomethyl groups can be introduced into the 4 and 5 positions of 1,2-dialkylbenzenes with high selectivity when the alkyl chains consist of two or more carbon atoms.

Process for the manufacture of 1,4-disubstituted bicyclic or tricyclic compounds and new 1,4-disubstituted bicyclic compounds

The present invention provides a new process for the manufacture of 1,4-disubstituted bicyclic or tricyclic compounds by reacting a 1,2-bis-cyanomethyl-benzene or 2,3-bis-cyanomethyl-naphthalene with glyoxal in the presence of a base and a solvent as well as new 1,4-disubstituted bicyclic compounds.