2-(Bromomethyl)benzaldehyde

95%

Reagent Code: #149703
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CAS Number 60633-91-2

science Other reagents with same CAS 60633-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.04 g/mol
Formula C₈H₇BrO
badge Registry Numbers
MDL Number MFCD17014845
thermostat Physical Properties
Boiling Point 264.6 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Density 1.524 g/cm3 at 25 °C (lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its reactive bromomethyl and aldehyde functional groups. The compound is particularly valuable in the preparation of heterocyclic compounds, such as benzoxepines and indole derivatives, which are common structural motifs in bioactive molecules. It also serves in the development of fluorescent probes and dyes, leveraging the aldehyde group for conjugation with other aromatic systems. Its versatility in organic transformations, including nucleophilic substitution and condensation reactions, makes it a preferred building block in medicinal chemistry and materials science.

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Test Parameter Specification
Appearance Brown Gray Powder
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,800.00
inventory 250mg
10-20 days ฿9,990.00
inventory 1g
10-20 days ฿30,430.00

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2-(Bromomethyl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its reactive bromomethyl and aldehyde functional groups. The compound is particularly valuable in the preparation of heterocyclic compounds, such as benzoxepines and indole derivatives, which are common structural motifs in bioactive molecules. It also serves in the development of fluorescent probes and dyes, leveraging the aldehyde group for conjugation with other aromatic systems. Its versatility in organic transfor

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its reactive bromomethyl and aldehyde functional groups. The compound is particularly valuable in the preparation of heterocyclic compounds, such as benzoxepines and indole derivatives, which are common structural motifs in bioactive molecules. It also serves in the development of fluorescent probes and dyes, leveraging the aldehyde group for conjugation with other aromatic systems. Its versatility in organic transformations, including nucleophilic substitution and condensation reactions, makes it a preferred building block in medicinal chemistry and materials science.

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