3-(Methoxymethoxy)benzaldehyde

95%(GC)

Reagent Code: #207890
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CAS Number 13709-05-2

science Other reagents with same CAS 13709-05-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.18 g/mol
Formula C₉H₁₀O₃
badge Registry Numbers
MDL Number MFCD04038425
inventory_2 Storage & Handling
Density 1.14
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceuticals and fine chemicals. It serves as a protected form of 3-hydroxybenzaldehyde, allowing selective reactions at other functional sites without interference from the phenolic group. The methoxymethyl (MOM) protecting group can be easily removed under mild acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the preparation of bioactive molecules, including drug candidates and agrochemicals, where controlled aldehyde reactivity and phenol protection are required. Also utilized in fragrance and flavor synthesis due to its aromatic aldehyde structure and stability under various reaction conditions.

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Test Parameter Specification
Appearance Colorless to light yellow clear liquid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,050.00
5g
10-20 days ฿7,960.00
3-(Methoxymethoxy)benzaldehyde
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Used as an intermediate in organic synthesis, particularly in pharmaceuticals and fine chemicals. It serves as a protected form of 3-hydroxybenzaldehyde, allowing selective reactions at other functional sites without interference from the phenolic group. The methoxymethyl (MOM) protecting group can be easily removed under mild acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the preparation of bioactive molecules, including drug candidates and agrochemicals, where contr

Used as an intermediate in organic synthesis, particularly in pharmaceuticals and fine chemicals. It serves as a protected form of 3-hydroxybenzaldehyde, allowing selective reactions at other functional sites without interference from the phenolic group. The methoxymethyl (MOM) protecting group can be easily removed under mild acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the preparation of bioactive molecules, including drug candidates and agrochemicals, where controlled aldehyde reactivity and phenol protection are required. Also utilized in fragrance and flavor synthesis due to its aromatic aldehyde structure and stability under various reaction conditions.

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