Methyl5-bromo-3,4-dimethoxy-2-methylbenzoate

95%

Reagent Code: #213827
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CAS Number 1809337-07-2

science Other reagents with same CAS 1809337-07-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.12 g/mol
Formula C₁₁H₁₃BrO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as an intermediate for bioactive molecules, particularly in the development of potential central nervous system agents. Its structure supports derivatization for use in medicinal chemistry research, especially in studies targeting neurological pathways. Also employed in organic synthesis to construct complex aromatic systems due to the reactivity of the bromo and ester functional groups. The compound's methoxy and methyl substitutions enhance lipophilicity, making it valuable in designing drug candidates with improved membrane permeability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿16,390.00
250mg
10-20 days ฿27,300.00
1g
10-20 days ฿54,600.00
Methyl5-bromo-3,4-dimethoxy-2-methylbenzoate
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Used in pharmaceutical synthesis as an intermediate for bioactive molecules, particularly in the development of potential central nervous system agents. Its structure supports derivatization for use in medicinal chemistry research, especially in studies targeting neurological pathways. Also employed in organic synthesis to construct complex aromatic systems due to the reactivity of the bromo and ester functional groups. The compound's methoxy and methyl substitutions enhance lipophilicity, making it valu

Used in pharmaceutical synthesis as an intermediate for bioactive molecules, particularly in the development of potential central nervous system agents. Its structure supports derivatization for use in medicinal chemistry research, especially in studies targeting neurological pathways. Also employed in organic synthesis to construct complex aromatic systems due to the reactivity of the bromo and ester functional groups. The compound's methoxy and methyl substitutions enhance lipophilicity, making it valuable in designing drug candidates with improved membrane permeability.

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