2-(Boc-oxyimino)-2-phenylacetonitrile

99%

Reagent Code: #80766
label
Alias 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile 2-Boc-oxyimino-2-phenylacetonitrile tert-Butylphenylacetonitrile oxime carboxylate
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CAS Number 58632-95-4

science Other reagents with same CAS 58632-95-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.26 g/mol
Formula C₁₃H₁₄N₂O₃
badge Registry Numbers
EC Number 261-370-9
MDL Number MFCD00001863
thermostat Physical Properties
Melting Point 85-88 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is primarily used as a protecting group reagent in organic synthesis, particularly for the protection of hydroxylamines. It is employed in the preparation of Boc-protected hydroxylamines, which are intermediates in the synthesis of various pharmaceuticals and bioactive compounds. The Boc group provides stability to the hydroxylamine during reactions, allowing for selective transformations without affecting other functional groups. Additionally, it is utilized in peptide synthesis to protect amino groups, ensuring the desired sequence and structure of the peptide chain. Its application is crucial in the development of drugs and complex organic molecules, where precise control over chemical reactions is essential.

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Test Parameter Specification
Melting Point 85-89
Purity (HPLC) 99-100
Appearance White to yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿490.00
inventory 25g
10-20 days ฿1,980.00
inventory 100g
10-20 days ฿7,590.00

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2-(Boc-oxyimino)-2-phenylacetonitrile
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This chemical is primarily used as a protecting group reagent in organic synthesis, particularly for the protection of hydroxylamines. It is employed in the preparation of Boc-protected hydroxylamines, which are intermediates in the synthesis of various pharmaceuticals and bioactive compounds. The Boc group provides stability to the hydroxylamine during reactions, allowing for selective transformations without affecting other functional groups. Additionally, it is utilized in peptide synthesis to protect

This chemical is primarily used as a protecting group reagent in organic synthesis, particularly for the protection of hydroxylamines. It is employed in the preparation of Boc-protected hydroxylamines, which are intermediates in the synthesis of various pharmaceuticals and bioactive compounds. The Boc group provides stability to the hydroxylamine during reactions, allowing for selective transformations without affecting other functional groups. Additionally, it is utilized in peptide synthesis to protect amino groups, ensuring the desired sequence and structure of the peptide chain. Its application is crucial in the development of drugs and complex organic molecules, where precise control over chemical reactions is essential.

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