2-(2-Nitrophenyl)propylcarbonochloridate

95%

Reagent Code: #220346
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CAS Number 179691-31-7

science Other reagents with same CAS 179691-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.64 g/mol
Formula C₁₀H₁₀ClNO₄
badge Registry Numbers
MDL Number MFCD11045267
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily as a reagent in organic synthesis, particularly in the protection of amines during peptide synthesis. It acts as a carbobenzyloxy (Cbz) protecting group equivalent, allowing selective modification of amino groups in complex molecules. Its nitro-substituted aromatic ring enhances reactivity and can also serve as a chromophore for monitoring reaction progress via UV detection. Commonly employed in the preparation of intermediates for pharmaceuticals and bioactive compounds where controlled activation and deprotection are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,200.00
inventory 1g
10-20 days ฿10,840.00
inventory 5g
10-20 days ฿27,370.00
inventory 250mg
10-20 days ฿5,140.00
inventory 10g
10-20 days ฿45,600.00
2-(2-Nitrophenyl)propylcarbonochloridate
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Used primarily as a reagent in organic synthesis, particularly in the protection of amines during peptide synthesis. It acts as a carbobenzyloxy (Cbz) protecting group equivalent, allowing selective modification of amino groups in complex molecules. Its nitro-substituted aromatic ring enhances reactivity and can also serve as a chromophore for monitoring reaction progress via UV detection. Commonly employed in the preparation of intermediates for pharmaceuticals and bioactive compounds where controlled a

Used primarily as a reagent in organic synthesis, particularly in the protection of amines during peptide synthesis. It acts as a carbobenzyloxy (Cbz) protecting group equivalent, allowing selective modification of amino groups in complex molecules. Its nitro-substituted aromatic ring enhances reactivity and can also serve as a chromophore for monitoring reaction progress via UV detection. Commonly employed in the preparation of intermediates for pharmaceuticals and bioactive compounds where controlled activation and deprotection are required.

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