O-(2-Methoxyisopropyl)hydroxylamine

95%(GC)(T)

Reagent Code: #221591
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CAS Number 103491-33-4

science Other reagents with same CAS 103491-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 105.14 g/mol
Formula C₄H₁₁NO₂
thermostat Physical Properties
Boiling Point 73°C|103mmHg(lit.)
inventory_2 Storage & Handling
Density 0.98
Storage 2-8°C, inert gas storage

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protecting group reagent for carbonyl compounds due to its ability to form stable oxime derivatives under mild conditions. Also employed in the synthesis of chiral amines through asymmetric reduction processes. Its methoxy-substituted alkyl chain enhances solubility and stability in various reaction media, making it suitable for use in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,990.00
inventory 1g
10-20 days ฿9,990.00

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O-(2-Methoxyisopropyl)hydroxylamine
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protecting group reagent for carbonyl compounds due to its ability to form stable oxime derivatives under mild conditions. Also employed in the synthesis of chiral amines through asymmetric reduction processes. Its methoxy-substituted alkyl chain enhances solubility and stability in various reaction media, making it suitable for use in multi-step synthetic routes.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a protecting group reagent for carbonyl compounds due to its ability to form stable oxime derivatives under mild conditions. Also employed in the synthesis of chiral amines through asymmetric reduction processes. Its methoxy-substituted alkyl chain enhances solubility and stability in various reaction media, making it suitable for use in multi-step synthetic routes.

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