2,3-Dimethoxybenzaldehyde oxime

95%

Reagent Code: #40697
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CAS Number 5470-95-1

science Other reagents with same CAS 5470-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.1900 g/mol
Formula C₉H₁₁NO₃
badge Registry Numbers
MDL Number MFCD00033234
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in drug development. Additionally, it finds application in the preparation of ligands for metal complexes used in catalytic processes. Its oxime functional group makes it useful in protecting carbonyl groups during multi-step synthetic procedures. In research, it is employed to study reaction mechanisms and to develop new chemical methodologies.

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Test Parameter Specification
Appearance Light Yellow Powder
Purity (%) 94.5-100%
NMR Conforms to Structure

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inventory 1g
10-20 days ฿603.00

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2,3-Dimethoxybenzaldehyde oxime
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in drug development. Additionally, it finds application in the preparation of ligands for metal complexes used in catalytic processes. Its oxime functional group makes it useful in protecting carbonyl groups during multi-step synthetic procedures. In research, it is employ

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of heterocyclic compounds, which are essential in drug development. Additionally, it finds application in the preparation of ligands for metal complexes used in catalytic processes. Its oxime functional group makes it useful in protecting carbonyl groups during multi-step synthetic procedures. In research, it is employed to study reaction mechanisms and to develop new chemical methodologies.

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