6209-00-3

Usage

Uses

Used in Organic Synthesis:
(E)-3-benzo[1,3]dioxol-5-yl-1-benzotriazol-1-yl-prop-2-en-1-one is used as a key intermediate in the synthesis of complex organic molecules, particularly due to its benzotriazole and benzodioxole functionalities. Its presence in the molecular structure can enhance the reactivity and selectivity of the compounds formed, making it a valuable component in the development of novel organic materials.
Used in Polymer Synthesis:
In the Polymer Industry, (E)-3-benzo[1,3]dioxol-5-yl-1-benzotriazol-1-yl-prop-2-en-1-one is used as a photoinitiator for the synthesis of polymers. Its ability to initiate polymerization reactions upon exposure to light makes it a promising candidate for the production of polymers with specific properties, such as those used in coatings, adhesives, and other industrial applications.
Used in Pharmaceutical Development:
(E)-3-benzo[1,3]dioxol-5-yl-1-benzotriazol-1-yl-prop-2-en-1-one is used as a building block in the development of new pharmaceuticals. Its unique chemical structure may contribute to the creation of novel drug candidates with potential therapeutic applications, pending further research into its biological activity and pharmacological properties.
Used in Agrochemical Development:
In the Agrochemical Industry, (E)-3-benzo[1,3]dioxol-5-yl-1-benzotriazol-1-yl-prop-2-en-1-one may be utilized in the design and synthesis of new agrochemicals, such as pesticides and herbicides. Its potential to form novel active ingredients could lead to the development of more effective and environmentally friendly products for agricultural use.

InChI:InChI=1/C16H11N3O3/c20-16(19-13-4-2-1-3-12(13)17-18-19)8-6-11-5-7-14-15(9-11)22-10-21-14/h1-9H,10H2/b8-6+

Upstream product

• 102076-70-0 DL-erythro-N-benzoyl-3-hydroxy-glutamic acid diethyl ester 
• 105-50-0 diethyl 1,3-acetonedicarboxylate 
• 7683-74-1 DL-erythro-3-hydroxy-glutamic acid diethyl ester; hydrochloride 
• 19883-13-7 diethyl N-acetyl-3-hydroxyglutamate 
• 97336-09-9 diethyl 2-acetamido-3-ketoglutarate 
• 996-75-8 diethyl 2-nitroso-3-ketoglutarate 
• 7683-73-0 diethyl 3-hydroxyglutamate 
• 97315-78-1 diethyl α-aminoacetonedicarboxylate 
• 7705-08-0 iron(III) chloride 
• 19883-13-7 DL-threo-N-acetyl-3-hydroxy-glutamic acid diethyl ester 

Downstream Products

• 107-43-7 betaine 
• 328-50-7 α-ketoglutaric acid 
• 7664-41-7 ammonia 

Relevant academic research and scientific papers

Kutznerides 1-4, depsipeptides from the actinomycete Kutzneria sp. 744 inhabiting mycorrhizal roots of Picea abies seedlings

Bioassay-guided fractionation of culture supernatants of the actinomycete Kutzneria sp. 744 resulted in the isolation of four new depsipeptides (1-4). Structure analysis revealed the general structure: cyclo[2-(1-methylcyclopropyl) -D-glycine-(2S,3aR,8aS)

L-threo- and L-erythro-3-Fluoroglutamic Acids. Synthesis by Fluorodehydroxylation and Enzymatic Resolution.

threo- and erythro-3-fluoroglutamic acids were prepared by fluorodehydroxylation of N-acetyl-3-hydroxyglutamic acids according to Kollonitsch.Following ion exchange column separation of the diastereoisomers, enzymatic deacylation by acylase I afforded optically pure L-isomers of the 3-fluoroglutamic acid.Assignment of structure was achieved by correlation with cis- and trans-3-fluoropyroglutamic acids.The results indicate predominant inversion of configuration during the fluorodehydroxylation reaction.