4-Phenyl-1,2,4-triazoline-3,5-dione

97%

Reagent Code: #119640
label
Alias PTAD;4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione
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CAS Number 4233-33-4

science Other reagents with same CAS 4233-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.15 g/mol
Formula C₈H₅N₃O₂
badge Registry Numbers
EC Number 224-191-7
MDL Number MFCD00003148
thermostat Physical Properties
Melting Point 165-170 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used primarily as a dienophile in Diels-Alder reactions, it facilitates the synthesis of complex organic compounds, particularly in the preparation of heterocyclic structures. Its high reactivity makes it valuable in polymer chemistry for cross-linking and modifying polymers to enhance their properties. Additionally, it is employed in organic synthesis to introduce phenyl and triazole groups into molecules, which can be useful in pharmaceutical and agrochemical research. The compound is also utilized in the study of reaction mechanisms due to its distinct reactivity pattern.

format_list_bulleted Product Specification

Test Parameter Specification
Carbon 52.9-56.8
Nitrogen 23.5-24.3
Purity (HPLC) 97-100
Appearance Red to red-orange or red-pink powder or crystals
Infrared Spectrum Conforms To Structure
NMR Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿480.00
inventory 1g
10-20 days ฿1,060.00
inventory 5g
10-20 days ฿4,350.00
inventory 100g
10-20 days ฿53,400.00
inventory 25g
10-20 days ฿15,440.00

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4-Phenyl-1,2,4-triazoline-3,5-dione
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Used primarily as a dienophile in Diels-Alder reactions, it facilitates the synthesis of complex organic compounds, particularly in the preparation of heterocyclic structures. Its high reactivity makes it valuable in polymer chemistry for cross-linking and modifying polymers to enhance their properties. Additionally, it is employed in organic synthesis to introduce phenyl and triazole groups into molecules, which can be useful in pharmaceutical and agrochemical research. The compound is also utilized in

Used primarily as a dienophile in Diels-Alder reactions, it facilitates the synthesis of complex organic compounds, particularly in the preparation of heterocyclic structures. Its high reactivity makes it valuable in polymer chemistry for cross-linking and modifying polymers to enhance their properties. Additionally, it is employed in organic synthesis to introduce phenyl and triazole groups into molecules, which can be useful in pharmaceutical and agrochemical research. The compound is also utilized in the study of reaction mechanisms due to its distinct reactivity pattern.

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