65678-12-8

Usage

InChI:InChI=1/C11H13ClO2/c1-11(2,3)8-4-7(6-13)5-9(12)10(8)14/h4-6,14H,1-3H3

Upstream product

• 13395-07-8 2-(tert-butyl)-6-chloro-4-methylphenol 
• 2409-55-4 2-tert-Butyl-4-methylphenol 
• 88-18-6 2-tert-Butylphenol 
• 65678-11-7 3-(1,1-Dimethylethyl)-4-hydroxy-benzaldehyde 

Downstream Products

• 103627-53-8 3-[1-(3-tert-Butyl-5-chloro-4-hydroxy-phenyl)-meth-(Z)-ylidene]-dihydro-furan-2-one 
• 65678-09-3 3-chloro-5-tert-butyl-4-hydroxybenzylidenemalononitrile 

Relevant academic research and scientific papers

OXIDATIVE COUPLING REACTION OF 2-HALOPHENOLS WITH K3Fe(CN)6 IN BENZENE SOLUTION

The oxidative coupling of twelve 2-halophenols (1a-1l) was carried out with K3Fe(CN)6 in benzene solution to obtain the corresponding dibenzofuran derivatives.However, only a small amount of the desired dibenzofurans such as 2,6-di-tert-butyl-8-methoxybenzofuran-1,4-quinone (9) and 4,8-di-tert-butyl-2,6-di-isopropyl-1-hydroxydibenzofuran (11) were obtained from 2-bromo-6-tert-butyl-4-methoxy- (1d) and 2-bromo-4-tert-butyl-6-isopropylphenol (1g), respectively.In the other cases, alternative type of products or tarry materials were formed.

Compositions for killing internal parasites containing 3-tert-alkyl-4-hydroxy-5-halo-benzylidene-malonitriles

A compound of the general formula I STR1 wherein R1 is halogen, R4 is a highly branched alkyl group, R2 and R3 which may be the same or different are hydrogen or halogen atoms or lower alkyl groups.