O-Acetyl-N-carbobenzoxyhydroxylamine

≥98%

Reagent Code: #121613
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CAS Number 180798-01-0

science Other reagents with same CAS 180798-01-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.2 g/mol
Formula C₁₀H₁₁NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

O-Acetyl-N-carbobenzoxyhydroxylamine is primarily used in organic synthesis as a protecting group for hydroxylamine derivatives. It helps stabilize hydroxylamine during complex chemical reactions, preventing unwanted side reactions. This compound is particularly useful in peptide synthesis and the preparation of hydroxamic acids, where selective protection and deprotection are crucial. Additionally, it finds application in the development of pharmaceutical intermediates, enabling the synthesis of compounds with potential therapeutic properties. Its role in facilitating controlled reactions makes it valuable in research and industrial processes.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 98-100%
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿960.00

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O-Acetyl-N-carbobenzoxyhydroxylamine
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O-Acetyl-N-carbobenzoxyhydroxylamine is primarily used in organic synthesis as a protecting group for hydroxylamine derivatives. It helps stabilize hydroxylamine during complex chemical reactions, preventing unwanted side reactions. This compound is particularly useful in peptide synthesis and the preparation of hydroxamic acids, where selective protection and deprotection are crucial. Additionally, it finds application in the development of pharmaceutical intermediates, enabling the synthesis of compoun

O-Acetyl-N-carbobenzoxyhydroxylamine is primarily used in organic synthesis as a protecting group for hydroxylamine derivatives. It helps stabilize hydroxylamine during complex chemical reactions, preventing unwanted side reactions. This compound is particularly useful in peptide synthesis and the preparation of hydroxamic acids, where selective protection and deprotection are crucial. Additionally, it finds application in the development of pharmaceutical intermediates, enabling the synthesis of compounds with potential therapeutic properties. Its role in facilitating controlled reactions makes it valuable in research and industrial processes.

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