29002-55-9

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 36, p. 1765, 1971 DOI: 10.1021/jo00812a009

InChI:InChI=1/C12H16Cl2/c1-7-8(2)10(4)12(6-14)11(5-13)9(7)3/h5-6H2,1-4H3

Upstream product

• 109-87-5 Dimethoxymethane 
• 488-23-3 1,2,3,4-Tetramethylbenzene 
• 50-00-0 formaldehyd 

Downstream Products

• 96579-20-3 1,2,3,4-Tetramethyl-5,6-bis-<(2,2-bis-methansulfonyloxymethyl)-propyl>-benzol 
• 94763-41-4 1,2,3,4-Tetramethyl-5,6-bis-<(2,2-bis-hydroxymethyl)-propyl>-benzol 
• 622390-96-9 1,2,3,4-Tetramethyl-5,6-bis-(2-prop-1-ynyl-phenoxymethyl)-benzene 
• 51207-63-7 2-Cyanomethyl-3,4,5,6-tetramethylbenzylcyanid 
• 70477-52-0 1,2,3,4-Tetramethyl-5,6-bis-thiocyanatomethyl-benzene 
• 31464-71-8 1,2-Diacetoxymethyl-3,4,5,6-tetramethylbenzen 
• 29328-74-3 1,2,3,4-Tetramethyl-5,6-bis-nitrooxymethyl-benzene 

Relevant academic research and scientific papers

The first immobilisation of glycoluril-based molecular clips on silica gel and alumina

The first example of immobilisation of some glycoluril-based molecular clips, which are good receptors for dihydroxybenzenes, on silica gel and alumina is described. 4,4'-Bis(methoxyphenyl)glycoluril was used as the base scaffold for the synthesis of mole

Glycoluril-derived crown clips as new ditopic receptors

Several new ditopic receptors have been synthesized from 4,4′-bis(methoxyphenyl)glycoluril (1). The first receptor site is a cleft composed of two fused 2-imidazolone rings, which are flanked by two aromatic side walls, and the second site is a crown ether moiety.

Studies on the Chemistry of Isoindoles and Isoindolenines, XXXVII. - Symmetrically Substituted 2-Alkyl-2H-isoindoles

2-Alkyl-Rn-2H-isoindoles (1; Rn = 4,5,6,7-tetramethyl, 4,5,6,7-tetrachloro) have been prepared efficiently by the N-oxide route and characterized by spectroscopic means.