2-bromoacetaldehyde

98%, 10% w/w in DCM

Reagent Code: #149654
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CAS Number 17157-48-1

science Other reagents with same CAS 17157-48-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 122.95 g/mol
Formula C₂H₃BrO
badge Registry Numbers
MDL Number MFCD01733508
thermostat Physical Properties
Melting Point 136-138 °C (lit.)
Boiling Point 93.7 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage -20°C, avoid light, argon-filled

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It plays a key role in the preparation of heterocyclic compounds due to its reactivity as an alkylating agent. Commonly employed in the synthesis of imidazoles, thiazoles, and other nitrogen-containing rings found in bioactive molecules. Also utilized in the manufacture of dyes and functionalized polymers where bromine serves as a leaving group for further substitution reactions. Its aldehyde group allows for condensation reactions, making it valuable in forming carbon-carbon bonds. Handle with care due to high reactivity and potential lachrymatory effects.

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Test Parameter Specification
Appearance liquid
Concentration 9-11
Solvent DCM
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿3,800.00
inventory 100mg
10-20 days ฿21,000.00
inventory 250mg
10-20 days ฿48,000.00
inventory 1g
10-20 days ฿169,900.00

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2-bromoacetaldehyde
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It plays a key role in the preparation of heterocyclic compounds due to its reactivity as an alkylating agent. Commonly employed in the synthesis of imidazoles, thiazoles, and other nitrogen-containing rings found in bioactive molecules. Also utilized in the manufacture of dyes and functionalized polymers where bromine serves as a leaving group for further substitution reactions. Its aldehyde group allows for condensation reactions, making it valuable in forming carbon-carbon bonds. Handle with care due to high reactivity and potential lachrymatory effects.
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