3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one

98%

Reagent Code: #56681
label
Alias 3-(diethoxyphosphoryloxy)-1,2,3-benzotriazin-4-one; 3-diethoxyphosphoryl-1,2,3-benzoxazole 4(3H)- Ketone
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CAS Number 165534-43-0

science Other reagents with same CAS 165534-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.22 g/mol
Formula C₁₁H₁₄N₃O₅P
badge Registry Numbers
MDL Number MFCD01236967
thermostat Physical Properties
Melting Point 75-77°C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This chemical is primarily used as a coupling reagent in peptide synthesis. It facilitates the formation of peptide bonds between amino acids, making it valuable in the production of peptides and proteins for research and pharmaceutical purposes. Additionally, it is employed in organic synthesis to activate carboxylic acids, enabling the formation of amides, esters, and other derivatives. Its efficiency and mild reaction conditions make it a preferred choice in laboratories focused on biochemistry and medicinal chemistry.

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Test Parameter Specification
Melting point 72-76
Purity (HPLC) 98-100
Appearance White to off-white crystalline powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,750.00
inventory 5g
10-20 days ฿720.00
inventory 100g
10-20 days ฿9,140.00

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3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one
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This chemical is primarily used as a coupling reagent in peptide synthesis. It facilitates the formation of peptide bonds between amino acids, making it valuable in the production of peptides and proteins for research and pharmaceutical purposes. Additionally, it is employed in organic synthesis to activate carboxylic acids, enabling the formation of amides, esters, and other derivatives. Its efficiency and mild reaction conditions make it a preferred choice in laboratories focused on biochemistry and me

This chemical is primarily used as a coupling reagent in peptide synthesis. It facilitates the formation of peptide bonds between amino acids, making it valuable in the production of peptides and proteins for research and pharmaceutical purposes. Additionally, it is employed in organic synthesis to activate carboxylic acids, enabling the formation of amides, esters, and other derivatives. Its efficiency and mild reaction conditions make it a preferred choice in laboratories focused on biochemistry and medicinal chemistry.

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