Di-tert-butyl tetrahydropyridazine-1,2-dicarboxylate

95%

Reagent Code: #180290
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CAS Number 340256-13-5

science Other reagents with same CAS 340256-13-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.37 g/mol
Formula C₁₄H₂₆N₂O₄
badge Registry Numbers
MDL Number MFCD09037886
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocyclic compounds. Its protected dihydropyridazine structure makes it valuable in pharmaceutical research for constructing complex molecules, including bioactive agents and functional materials. The tert-butyl groups provide steric protection, allowing selective reactions at other sites in the molecule, which is advantageous in multi-step synthesis. It is also employed in the development of novel catalysts and ligands due to its stable yet reactive framework.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,750.00
inventory 5g
10-20 days ฿41,860.00
inventory 250mg
10-20 days ฿4,400.00

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Di-tert-butyl tetrahydropyridazine-1,2-dicarboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocyclic compounds. Its protected dihydropyridazine structure makes it valuable in pharmaceutical research for constructing complex molecules, including bioactive agents and functional materials. The tert-butyl groups provide steric protection, allowing selective reactions at other sites in the molecule, which is advantageous in multi-step synthesis. It is also employed in the development of novel

Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocyclic compounds. Its protected dihydropyridazine structure makes it valuable in pharmaceutical research for constructing complex molecules, including bioactive agents and functional materials. The tert-butyl groups provide steric protection, allowing selective reactions at other sites in the molecule, which is advantageous in multi-step synthesis. It is also employed in the development of novel catalysts and ligands due to its stable yet reactive framework.

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