(2S,5R)-1-Boc-2,5-dimethylpiperazine hydrochloride

95%

Reagent Code: #36584
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CAS Number 1374975-96-8

science Other reagents with same CAS 1374975-96-8

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Weight 250.7655 g/mol
Formula C₁₁H₂₃ClN₂O₂
badge Registry Numbers
MDL Number MFCD13191717
inventory_2 Storage & Handling
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description Product Description

This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with piperazine-based structures. It serves as a key intermediate in the production of drugs targeting central nervous system disorders, such as antipsychotics and antidepressants. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions during synthesis, enabling precise modifications to the piperazine ring. Additionally, its chiral centers make it valuable in creating enantioselective compounds, which are crucial for drugs requiring specific stereochemistry for efficacy and safety. Its hydrochloride form enhances solubility, facilitating its use in various chemical reactions and formulations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,485.00

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(2S,5R)-1-Boc-2,5-dimethylpiperazine hydrochloride
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This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with piperazine-based structures. It serves as a key intermediate in the production of drugs targeting central nervous system disorders, such as antipsychotics and antidepressants. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions during synthesis, enabling precise modifications to the piperazine ring. Additionally, its chiral centers

This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with piperazine-based structures. It serves as a key intermediate in the production of drugs targeting central nervous system disorders, such as antipsychotics and antidepressants. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions during synthesis, enabling precise modifications to the piperazine ring. Additionally, its chiral centers make it valuable in creating enantioselective compounds, which are crucial for drugs requiring specific stereochemistry for efficacy and safety. Its hydrochloride form enhances solubility, facilitating its use in various chemical reactions and formulations.

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