Methyl 4-bromo-2-formylbenzoate

95%

Reagent Code: #47406
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CAS Number 1260795-42-3

science Other reagents with same CAS 1260795-42-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.0500 g/mol
Formula C₉H₇BrO₃
badge Registry Numbers
MDL Number MFCD16036574
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 pharmaceuticals and agrochemicals. Its functional groups, including the formyl and ester moieties, make it versatile for further chemical modifications, such as coupling reactions or transformations into heterocyclic compounds. It is particularly valuable in the development of active ingredients for drugs targeting specific biological pathways. Additionally, it finds application in material science for creating specialized polymers or coatings with tailored properties. Its bromo substituent allows for further functionalization through cross-coupling reactions, enhancing its utility in complex synthetic routes.

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Test Parameter Specification
Appearance White to Off-White to Light Yellow to Yellow Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,695.00

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Methyl 4-bromo-2-formylbenzoate
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its functional groups, including the formyl and ester moieties, make it versatile for further chemical modifications, such as coupling reactions or transformations into heterocyclic compounds. It is particularly valuable in the development of active ingredients for drugs targeting specific biological pathways. Additionally, it finds application in material science for cr

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its functional groups, including the formyl and ester moieties, make it versatile for further chemical modifications, such as coupling reactions or transformations into heterocyclic compounds. It is particularly valuable in the development of active ingredients for drugs targeting specific biological pathways. Additionally, it finds application in material science for creating specialized polymers or coatings with tailored properties. Its bromo substituent allows for further functionalization through cross-coupling reactions, enhancing its utility in complex synthetic routes.

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