89863-03-6

Usage

Structure

Cyclic ether with a nitrophenyl group attached to the second carbon atom

Usage

a. Organic synthesis
b. Reagent in chemical reactions

Properties

a. Antibacterial
b. Antifungal

Potential applications

a. Pharmaceuticals
b. Biotechnology

Safety precautions

a. May cause skin irritation
b. May cause eye irritation
c. May cause respiratory irritation
d. Harmful if ingested
e. Harmful if inhaled

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 56-81-5 glycerol 

Downstream Products

• 89863-04-7 2-p-nitrophenyl-1,3-dioxan-5-yl p-aminobenzoate 
• 89863-02-5 4-{[1-(4-Nonyloxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 
• 89863-01-4 4-{[1-(4-Octyloxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 
• 89863-00-3 4-{[1-(4-Heptyloxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 
• 89862-99-7 4-{[1-(4-Hexyloxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 
• 89862-98-6 2-p-nitrophenyl-1,3-dioxan-5-yl 4-(4-pentyloxybenzylideneamino)benzoate 
• 89862-97-5 4-{[1-(4-Butoxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 
• 89862-96-4 4-{[1-(4-Propoxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 
• 89862-95-3 4-{[1-(4-Ethoxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 
• 89862-94-2 4-{[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid 2-(4-nitro-phenyl)-[1,3]dioxan-5-yl ester 

Relevant academic research and scientific papers

Modified boehmite: A choice of catalyst for the selective conversion of glycerol to five-membered dioxolane

The choice of the active site and support matrix decides the activity of a catalyst. Any modifications on these will have a significant impact on the reactivity and selectivity of the catalyst. Here, we have synthesised WO3-loaded boehmite and applied it for the acetalization of a biomass-derived bulk chemical, glycerol. The well-characterized acid catalyst exhibits a selective acetalization of glycerol with good conversions into a five-membered dioxolane product. The cyclability of the catalyst up to six times along with the retention of the catalytic activity ensures the heterogeneity of the material.

SYNTHESIS OF DERIVATIVES OF 1,3-DIOXANE WITH MESOMORPHOUS CHARACTERISTICS

2-p-Nitrophenyl-1,3-dioxan-5-yl 4-(4-alkoxybenzylideneamino)benzoates were sythesized.They possess the characteristics of smectic and nematic liquid crystals in the range of 90-221 deg C.