2798-05-2

Usage

Uses

Used in Polymer and Plastics Industry:
4,4'-DIISOTHIOCYANATODIPHENYLMETHANE is used as a crosslinking agent for enhancing the strength and durability of polymers and plastics. Its ability to form strong bonds with other molecules contributes to the improved performance and longevity of these materials.
Used as a Curing Agent for Epoxy Resins:
In the epoxy resins industry, 4,4'-DIISOTHIOCYANATODIPHENYLMETHANE is used as a curing agent to harden and set the epoxy, resulting in a solid, stable material with a wide range of applications, including adhesives, coatings, and composites.
Used in the Synthesis of Organic Compounds:
4,4'-DIISOTHIOCYANATODIPHENYLMETHANE is used as a building block in the synthesis of various organic compounds, contributing to the development of new chemical products and innovations in the chemical industry.
Used in the Development of New Materials and Coatings:
4,4'-DIISOTHIOCYANATODIPHENYLMETHANE has been studied for potential applications in the development of new materials and coatings, where its crosslinking properties can be utilized to create advanced materials with unique properties and improved performance.

Upstream product

• 2915-44-8 4,4'-diazidodiphenylmethane 
• 75-15-0 carbon disulfide 
• 1006367-90-3 4,4'-diiminophosphorodiphenylmethane 
• 101-77-9 4,4'-diamino diphenyl methane 
• 102368-13-8 1,1'-Thiocarbonyldi-2(1H)-pyridone 
• 121711-44-2 C₁₇H₁₈N₂S₄ 

Downstream Products

• 147199-35-7 C₂₇H₂₄N₄S₂ 
• 1570231-78-5 C₆₉H₈₀N₁₂O₆S₂ 
• 95296-93-8 5,5'-(4,4'-methanediyl-dianilino)-bis-[1,2,3,4]thiatriazole 
• 100456-79-9 4,4'-Bis--diphenylmethan 
• 97376-64-2 4,4'-di(3-thiosemicarbazide)biphenylmethane 

Relevant academic research and scientific papers

Synthesis and insecticidal activity of N,N'-bis (3-substituted thiourea) methylenedianiline derivatives

Bis thiourea derivatives (5a-e) were synthesized by the treatment of diisothiocyanate (4) with various secondary amines and anilines. The structures of the compounds (5a- e) were confirmed by their spectral analysis. The insecticidal activity of the diisothicoyanate (4) and bisthiourea derivatives (5a-e) were studied and found to be better activities in comparison with the standard drug.

Polythioureas: Main chain chiral polymers in hydride transfer hydrogenation

Chiral polythioureas have been synthesized and tested in asymmetric hydride transfer reduction of ketones with ruthenium. With polyurea 18, 70% ee was attained for acetophenone reduction; after filtration, it can be reused at least four times without any detectable loss of activity and only a slight decrease in selectivity. Various aryl alkyl ketones were reduced with the same system and up to 84% ee was measured with isopropyl phenyl ketone.

A FACILE NEW METHOD FOR THE PREPARATION OF AROMATIC DIISOTHIOCYANATES

In the present communication we describe a new facile method for the preparation of aromatic diisothiocyanates.The main advantage of this method is a one-pot procedure from bis(dithiocarbamates) compared with the methods described in the literature.