Methyl4-(benzyloxy)-3-methoxy-2-nitrobenzoate

95%

Reagent Code: #213365
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CAS Number 1461706-26-2

science Other reagents with same CAS 1461706-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.29 g/mol
Formula C₁₆H₁₅NO₆
badge Registry Numbers
MDL Number MFCD26407791
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its functional groups—nitro, methoxy, and benzyloxy—allow for selective transformations, such as reduction of the nitro group to an amine, which can then participate in further coupling reactions. Commonly employed in the development of analgesic and anti-inflammatory agents due to its structural similarity to known active scaffolds. Also utilized in the synthesis of natural product analogs and in medicinal chemistry research for building complex aromatic frameworks.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,460.00
inventory 250mg
10-20 days ฿16,080.00
inventory 1g
10-20 days ฿53,300.00
Methyl4-(benzyloxy)-3-methoxy-2-nitrobenzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its functional groups—nitro, methoxy, and benzyloxy—allow for selective transformations, such as reduction of the nitro group to an amine, which can then participate in further coupling reactions. Commonly employed in the development of analgesic and anti-inflammatory agents due to its structural similarity to known active scaffolds. Also utilized in the synthesis of natural product a

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. Its functional groups—nitro, methoxy, and benzyloxy—allow for selective transformations, such as reduction of the nitro group to an amine, which can then participate in further coupling reactions. Commonly employed in the development of analgesic and anti-inflammatory agents due to its structural similarity to known active scaffolds. Also utilized in the synthesis of natural product analogs and in medicinal chemistry research for building complex aromatic frameworks.

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