2-Nitrobenzaldoxime [Deprotecting Agent]

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Reagent Code: #86342
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CAS Number 6635-41-2

science Other reagents with same CAS 6635-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.13 g/mol
Formula C₇H₆N₂O₃
badge Registry Numbers
MDL Number MFCD00007187
thermostat Physical Properties
Boiling Point 305.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily as a deprotecting agent in organic synthesis, it selectively removes protecting groups from molecules, enabling the continuation of complex chemical reactions. Its application is crucial in peptide synthesis, where it helps in the stepwise assembly of amino acids without disrupting the integrity of the peptide chain. Additionally, it finds use in the preparation of pharmaceuticals, where precise deprotection is necessary to achieve the desired drug structure. Its efficiency and specificity make it a valuable tool in the development of active pharmaceutical ingredients (APIs) and other fine chemicals.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿864.00
inventory 25g
10-20 days ฿3,789.00
inventory 100g
10-20 days ฿14,625.00

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2-Nitrobenzaldoxime [Deprotecting Agent]
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Used primarily as a deprotecting agent in organic synthesis, it selectively removes protecting groups from molecules, enabling the continuation of complex chemical reactions. Its application is crucial in peptide synthesis, where it helps in the stepwise assembly of amino acids without disrupting the integrity of the peptide chain. Additionally, it finds use in the preparation of pharmaceuticals, where precise deprotection is necessary to achieve the desired drug structure. Its efficiency and specificity

Used primarily as a deprotecting agent in organic synthesis, it selectively removes protecting groups from molecules, enabling the continuation of complex chemical reactions. Its application is crucial in peptide synthesis, where it helps in the stepwise assembly of amino acids without disrupting the integrity of the peptide chain. Additionally, it finds use in the preparation of pharmaceuticals, where precise deprotection is necessary to achieve the desired drug structure. Its efficiency and specificity make it a valuable tool in the development of active pharmaceutical ingredients (APIs) and other fine chemicals.

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