6-bromochroman-2-carboxylic acid

≥95%

Reagent Code: #143926
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CAS Number 99199-54-9

science Other reagents with same CAS 99199-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.08 g/mol
Formula C₁₀H₉BrO₃
badge Registry Numbers
MDL Number MFCD07778356
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential cardiovascular and central nervous system activity. Its chroman structure supports the creation of chroman-based derivatives, which are found in antioxidants, receptor modulators, and anti-inflammatory agents. The bromine substituent at the 6-position facilitates further functionalization via cross-coupling reactions, enabling the synthesis of diverse analogs for structure-activity relationship studies. Commonly employed in medicinal chemistry for constructing heterocyclic frameworks in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,600.00
inventory 250mg
10-20 days ฿7,660.00
inventory 1g
10-20 days ฿20,140.00
inventory 5g
10-20 days ฿76,290.00

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6-bromochroman-2-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential cardiovascular and central nervous system activity. Its chroman structure supports the creation of chroman-based derivatives, which are found in antioxidants, receptor modulators, and anti-inflammatory agents. The bromine substituent at the 6-position facilitates further functionalization via cross-coupling reactions, enabling the synthesis of diverse analogs for str

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential cardiovascular and central nervous system activity. Its chroman structure supports the creation of chroman-based derivatives, which are found in antioxidants, receptor modulators, and anti-inflammatory agents. The bromine substituent at the 6-position facilitates further functionalization via cross-coupling reactions, enabling the synthesis of diverse analogs for structure-activity relationship studies. Commonly employed in medicinal chemistry for constructing heterocyclic frameworks in drug discovery programs.

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