O-(p-Tolylsulfonyl)hydroxylamine

95%

Reagent Code: #222004
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CAS Number 52913-14-1

science Other reagents with same CAS 52913-14-1

blur_circular Chemical Specifications

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Weight 187.22 g/mol
Formula C₇H₉NO₃S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an electrophilic aminating agent in organic synthesis, enabling the direct introduction of nitrogen into carbon nucleophiles such as enolates, organometallic reagents, and activated aromatic systems. It is particularly valuable for the preparation of hydrazine derivatives and α-amino carbonyl compounds. Its reactivity allows for selective amination under mild conditions, making it useful in pharmaceutical and agrochemical synthesis where nitrogen-containing structures are prevalent. The compound facilitates efficient bond formation in heterocycle synthesis and is employed in the development of bioactive molecules and functional materials.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿10,250.00

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O-(p-Tolylsulfonyl)hydroxylamine
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Used primarily as an electrophilic aminating agent in organic synthesis, enabling the direct introduction of nitrogen into carbon nucleophiles such as enolates, organometallic reagents, and activated aromatic systems. It is particularly valuable for the preparation of hydrazine derivatives and α-amino carbonyl compounds. Its reactivity allows for selective amination under mild conditions, making it useful in pharmaceutical and agrochemical synthesis where nitrogen-containing structures are prevalent. The

Used primarily as an electrophilic aminating agent in organic synthesis, enabling the direct introduction of nitrogen into carbon nucleophiles such as enolates, organometallic reagents, and activated aromatic systems. It is particularly valuable for the preparation of hydrazine derivatives and α-amino carbonyl compounds. Its reactivity allows for selective amination under mild conditions, making it useful in pharmaceutical and agrochemical synthesis where nitrogen-containing structures are prevalent. The compound facilitates efficient bond formation in heterocycle synthesis and is employed in the development of bioactive molecules and functional materials.

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