4-Cbz-piperazine-1-carbonyl Chloride

95%

Reagent Code: #162391
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CAS Number 25539-27-9

science Other reagents with same CAS 25539-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.72 g/mol
Formula C₁₃H₁₅ClN₂O₃
badge Registry Numbers
MDL Number MFCD09743772
thermostat Physical Properties
Boiling Point 203-208 °C(Press:1.3Torr)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where piperazine rings are required. Its main application lies in peptide coupling and the construction of complex heterocyclic systems. The Cbz-protected piperazine moiety allows selective reactivity at another site of the molecule, making it valuable in multi-step organic syntheses. It is especially useful in medicinal chemistry for creating protease inhibitors, receptor antagonists, and kinase inhibitors. Due to the presence of the carbonyl chloride group, it readily reacts with amines and alcohols to form amides and esters, enabling efficient derivatization. Its stability under various reaction conditions and ease of deprotection make it a preferred building block in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,250.00
inventory 1g
10-20 days ฿19,230.00

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4-Cbz-piperazine-1-carbonyl Chloride
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where piperazine rings are required. Its main application lies in peptide coupling and the construction of complex heterocyclic systems. The Cbz-protected piperazine moiety allows selective reactivity at another site of the molecule, making it valuable in multi-step organic syntheses. It is especially useful in medicinal chemistry for creating proteas

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where piperazine rings are required. Its main application lies in peptide coupling and the construction of complex heterocyclic systems. The Cbz-protected piperazine moiety allows selective reactivity at another site of the molecule, making it valuable in multi-step organic syntheses. It is especially useful in medicinal chemistry for creating protease inhibitors, receptor antagonists, and kinase inhibitors. Due to the presence of the carbonyl chloride group, it readily reacts with amines and alcohols to form amides and esters, enabling efficient derivatization. Its stability under various reaction conditions and ease of deprotection make it a preferred building block in drug discovery and development.

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