247575-33-3

Upstream product

• 247575-32-2 3-bromo-2,5-dimethylbenzonitrile 
• 66788-13-4 2,6-dibromo-1,4-dimethylbenzene 
• 95-78-3 2,5-Dimethylaniline 
• 26829-89-0 2,4-dibromo-3,6-dimethylaniline 

Downstream Products

• 247575-34-4 1-bromo-2,5-dimethyl-3-hydroxymethylbenzene 
• 247575-39-9 1,2-bis-(3'-bromomethyl-2',5'-dimethylphenyl)ethane 
• 247575-38-8 1,2-bis-(3'-hydroxymethyl-2',5'-dimethylphenyl)ethane 
• 247575-28-6 1,2-bis-(3'-cyano-2',5'-dimethylphenyl)ethane 
• 247575-37-7 1,2-bis-(3'-formyl-2',5'-dimethylphenyl)ethane 
• 247575-36-6 1,2-bis-(3'-bromo-2',5'-dimethylphenyl)ethane 
• 247575-35-5 1-bromo-3-bromomethyl-2,5-dimethylbenzene 
• 663941-21-7 7-hydroxy-4-methyl-bicyclo[4.2.0]octa-1,3,5-triene-2-carbonitrile 

Relevant academic research and scientific papers

Synthesis, reactions, and structural and NMR features of [2.2]metacyclophane monoenes and their tricarbonylchromium and cyclopentadienyliron(+) complexes

8,16-Dimethyl-, 5,8,13,16-tetramethyl-, and 4,6,8,12,14,16- hexamethyl[2.2]metacyclophanene have been synthesized from the corresponding methyl-substituted 3-thia[3.2]metacyclophane precursors via a Wittig rearrangement-Hofmann elimination procedure. Simp