1,3,4,6-Tetrachloro-3a,6a-diphenylglycouril

CARBON 44%-45%

Reagent Code: #242422
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CAS Number 51592-06-4

science Other reagents with same CAS 51592-06-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 432.09 g/mol
Formula C₁₆HCl₄N₄O₂
badge Registry Numbers
MDL Number MFCD00027367
thermostat Physical Properties
Melting Point 249-252  °C (lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a chlorinating agent in organic synthesis, this compound efficiently transfers chlorine atoms to various substrates, making it valuable in the preparation of chlorinated organic compounds. It is particularly effective in the chlorination of alkenes, alcohols, and carbonyl compounds under mild conditions. Due to its stability and selectivity, it serves as a reagent in pharmaceutical and agrochemical manufacturing where controlled chlorination is required. Additionally, it has been employed in polymer chemistry for modifying polymer structures through chlorination, enhancing flame retardancy and thermal stability. Its solid form and ease of handling make it preferable over gaseous or liquid chlorinating agents in industrial processes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,850.00
inventory 250mg
10-20 days ฿26,100.00
inventory 1g
10-20 days ฿76,500.00

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1,3,4,6-Tetrachloro-3a,6a-diphenylglycouril
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Used primarily as a chlorinating agent in organic synthesis, this compound efficiently transfers chlorine atoms to various substrates, making it valuable in the preparation of chlorinated organic compounds. It is particularly effective in the chlorination of alkenes, alcohols, and carbonyl compounds under mild conditions. Due to its stability and selectivity, it serves as a reagent in pharmaceutical and agrochemical manufacturing where controlled chlorination is required. Additionally, it has been employ

Used primarily as a chlorinating agent in organic synthesis, this compound efficiently transfers chlorine atoms to various substrates, making it valuable in the preparation of chlorinated organic compounds. It is particularly effective in the chlorination of alkenes, alcohols, and carbonyl compounds under mild conditions. Due to its stability and selectivity, it serves as a reagent in pharmaceutical and agrochemical manufacturing where controlled chlorination is required. Additionally, it has been employed in polymer chemistry for modifying polymer structures through chlorination, enhancing flame retardancy and thermal stability. Its solid form and ease of handling make it preferable over gaseous or liquid chlorinating agents in industrial processes.

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