4-chloro-2-fluoro-3-methoxybenzaldehyde

97%

Reagent Code: #162298
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CAS Number 1002344-97-9

science Other reagents with same CAS 1002344-97-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.58 g/mol
Formula C₈H₆ClFO₂
badge Registry Numbers
MDL Number MFCD19687172
inventory_2 Storage & Handling
Storage 2-8 °C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. Its functional groups enable selective reactions, making it valuable in constructing complex aromatic molecules. Also employed in agrochemical synthesis for creating herbicides and fungicides due to its halogenated structure, which enhances bioactivity. Commonly utilized in research and development for designing novel organic compounds in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿8,280.00
5g
10-20 days ฿26,650.00
4-chloro-2-fluoro-3-methoxybenzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. Its functional groups enable selective reactions, making it valuable in constructing complex aromatic molecules. Also employed in agrochemical synthesis for creating herbicides and fungicides due to its halogenated structure, which enhances bioactivity. Commonly utilized in research an

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting central nervous system disorders and anti-inflammatory agents. Its functional groups enable selective reactions, making it valuable in constructing complex aromatic molecules. Also employed in agrochemical synthesis for creating herbicides and fungicides due to its halogenated structure, which enhances bioactivity. Commonly utilized in research and development for designing novel organic compounds in medicinal chemistry.

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