26112-94-7

Usage

Uses

Used in Adhesives Industry:
1-(3-Phenyl-2-propenoyl)-1H-benzotriazole is used as a photoinitiator for the production of adhesives. It facilitates the polymerization process, enabling the crosslinking of monomers or oligomers when exposed to ultraviolet light. This enhances the adhesive's bonding strength and durability.
Used in Coatings Industry:
In the coatings industry, 1-(3-Phenyl-2-propenoyl)-1H-benzotriazole is used as a photoinitiator to promote the curing of coatings. Its high absorption in the UV region allows for efficient polymerization, resulting in coatings with improved hardness, chemical resistance, and durability. Additionally, its low yellowing effect makes it an ideal choice for clear coatings, ensuring that the final product maintains its color and appearance over time.
Used in Printing Inks Industry:
1-(3-Phenyl-2-propenoyl)-1H-benzotriazol is also utilized as a photoinitiator in the production of printing inks. It aids in the polymerization process, ensuring that the ink cures quickly and effectively when exposed to ultraviolet light. This results in high-quality prints with excellent adhesion, durability, and resistance to various environmental factors.
Overall, 1-(3-Phenyl-2-propenoyl)-1H-benzotriazol, or BAPO, is a crucial component in the manufacturing of UV-curable products across various industries, including adhesives, coatings, and printing inks. Its versatility, efficiency, and low yellowing effect make it a highly desirable photoinitiator for these applications.

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 621-82-9 Cinnamic acid 

Downstream Products

• 1088979-90-1 [(2-(N-methyl-N-benzylamino)phenyl)(3-phenylpropenoyl)methylidene](triphenyl)phosphorane 
• 14776-43-3 2,5-diphenylpyrazolidin-3-one 
• 1097651-77-8 2-(4-chlorophenyl)-5-phenylpyrazolidin-3-one 
• 1097651-70-1 5-phenyl-2-(p-tolyl)pyrazolidin-3-one 
• 1097651-78-9 2-(4-bromophenyl)-5-phenylpyrazolidin-3-one 
• 16619-19-5 4-cinnamoylmorpholine 
• 53691-91-1 N-(4-chlorophenyl)-3-phenylacrylamide 
• 76228-15-4 N-(4-methoxyphenyl)-3-phenylacrylamide 
• 6299-56-5 N-(β-phenylacroyl)butylamine 
• 3056-73-3 cinnamanilide 
• 1198081-28-5 C₂₁H₂₀N₄O₃ 

Relevant academic research and scientific papers

TCT-mediated synthesis of N-acylbenzotriazoles in aqueous media

The synthesis of N-acylbenzotriazoles has been demonstrated by the 2,4,6-trichloro-1,3,5-triazine (TCT)-mediated condensation of carboxylic acids with 1H-benzotriazole in aqueous media. In saturated aqueous sodium bicarbonate, TCT was found to be relatively stable and functioned as an efficient acid activator in the acyl transfer process. This operationally simple and economic method allows the scalable synthesis of N-acylbenzotriazoles in good to excellent yields.

Facile synthesis of N-acylbenzotriazoles from carboxylic acids mediated by 2,4,6-trichloro-1,3,5-triazine and triethylamine

Abstract A facile, efficient, and economic method toward N-acylbenzotriazoles was reported using 2,4,6-trichloro-1,3,5-triazine in combination with triethylamine as a carboxylic acid activator. Through reacting 1H-benzotriazole with the generated triacylated triazine intermediate, a series of N-acylbenzotriazoles could be rapidly prepared in high yields without column chromatography.

CINNAMOYL INHIBITORS OF TRANSGLUTAMINASE

A compound of Formula, (I) or Formula: (II)

New gas-phase cascade reactions of stabilized phosphorus ylides leading to ring-fused indoles and to quinolines

(Chemical Equation Presented) Gas-phase cyclization processes of stabilized phosphorus ylides bearing a suitably substituted 2-aminophenyl group lead efficiently either to 3-substituted quinolines or benzo[c]-carbazole and heterocyclic-fused analogues depending on the substituents present.