4066-30-2

Usage

Physical state

Yellow crystalline solid

Primary use

Precursor for dyes, pigments, and other organic compounds

Known for

Strong color

Application

Used as a dye intermediate in the production of various colored materials

Usage

Research and laboratory settings as a reagent for organic synthesis and as a building block for the creation of more complex chemical compounds

Potential applications

Pharmaceutical and materials science due to its unique structure and properties.

Upstream product

• 118-75-2 chloranil 
• 108-95-2 phenol 
• 139-02-6 sodium phenoxide 
• 100-67-4 potassium phenolate 

Downstream Products

• 4066-31-3 2,5-bis-aziridin-1-yl-3,6-diphenoxy-[1,4]benzoquinone 

Relevant academic research and scientific papers

Photoreactivity of some 2-alkoxy/phenoxy-3,5,6-tri-chloro/bromo-1,4-benzoquinones

We report the reaction between 2,3,5,6-tetrachloro/bromo-1,4-benzoquinones (5A/B) with deprotonated alkoholes/phenoles 7a-e to give yellow 2-alkoxy/phenoxy-3,5,6-trichloro/bromo-1,4-benzoquinones 9A/Ba-e. These reaction products are probably photodegraded yielding the corresponding 2-hydroxy-3,5,6-trichloro/bromo-1,4-benzoquinones 15A/B. The quinones 9A/B are not O-conjugated dehydrated, and the quinones 9Ba-e are not C-3-debrominated. These reactions are observed by photodegradation from 2-dialkylamino-3,5,6-trichloro/bromo-1,4-benzoquinones.

Reactive dyestuffs

Triphendioxazine reactive dyestuffs of the general formula STR1 with the substituent definition given in the description, are outstandingly suitable for dyeing and printing materials containing hydroxyl groups or amide groups. They give red dyeings with high wet- and light-fastnesses.

Triphendioxazine dyestuffs

Triphendioxazine dyestuffs of the formula STR1 having the substituent meanings specified in the descriptive part, are highly suitable for dyeing and printing hydroxyl- or amido-containing materials, in particular fibre materials, and produce wash-fast dyeings and prints.