2-Bromo-6-chlorobenzaldehyde

97%

Reagent Code: #144249
label
Alias 2-bromo-6-chlorobenzaldehyde; 2-chloro-6-bromo-benzaldehyde;
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CAS Number 64622-16-8

science Other reagents with same CAS 64622-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.46 g/mol
Formula C₇H₄BrClO
thermostat Physical Properties
Boiling Point 258.819ºC
inventory_2 Storage & Handling
Density 1.698g/cm3
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of reactive halogen atoms and an aldehyde group, enabling functionalization through cross-coupling reactions, nucleophilic substitution, and condensation processes. Commonly employed in the development of active ingredients in crop protection agents and in the preparation of substituted benzene derivatives for medicinal chemistry research.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 96.5-100
Melting Point 81-86°C
Appearance SOLID

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿180.00
5g
10-20 days ฿950.00
25g
10-20 days ฿3,820.00
100g
10-20 days ฿14,890.00
500g
10-20 days ฿74,120.00
2-Bromo-6-chlorobenzaldehyde
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of reactive halogen atoms and an aldehyde group, enabling functionalization through cross-coupling reactions, nucleophilic substitution, and condensation processes. Commonly employed in the development of active ingredients in crop protection agents and in the preparation of substituted benzene

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions due to the presence of reactive halogen atoms and an aldehyde group, enabling functionalization through cross-coupling reactions, nucleophilic substitution, and condensation processes. Commonly employed in the development of active ingredients in crop protection agents and in the preparation of substituted benzene derivatives for medicinal chemistry research.

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