3-Bromo-2-methoxybenzaldehyde

95%

Reagent Code: #145197
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CAS Number 88275-87-0

science Other reagents with same CAS 88275-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.04 g/mol
Formula C₈H₇BrO₂
thermostat Physical Properties
Boiling Point 282.3°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require substituted benzaldehyde derivatives. Its functional groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the production of herbicides and fungicides due to its reactivity and structural properties. Also utilized in research laboratories for the preparation of heterocyclic compounds and in the construction of more complex aldehydes through cross-coupling reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,600.00
5g
10-20 days ฿6,400.00
25g
10-20 days ฿24,000.00
3-Bromo-2-methoxybenzaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require substituted benzaldehyde derivatives. Its functional groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the production of herbicides and fungicides due to its reactivity and structural properties. Also utilized in research laboratories for the preparation of heterocyclic compounds and in the constru
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require substituted benzaldehyde derivatives. Its functional groups allow for selective reactions, making it valuable in creating complex organic molecules. Commonly employed in the production of herbicides and fungicides due to its reactivity and structural properties. Also utilized in research laboratories for the preparation of heterocyclic compounds and in the construction of more complex aldehydes through cross-coupling reactions.
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