(S)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acid

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Reagent Code: #113664
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CAS Number 159532-59-9

science Other reagents with same CAS 159532-59-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.26 g/mol
Formula C₁₀H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD02179105
thermostat Physical Properties
Melting Point 243-247°C (dec.)
Boiling Point 371.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This chemical is primarily used as an intermediate in the synthesis of pharmaceutical compounds. It plays a crucial role in the production of various active pharmaceutical ingredients (APIs), particularly those involving piperazine derivatives. Its structure is valuable in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, it is utilized in peptide synthesis, where it helps in building complex peptide chains by providing a protected carboxylic acid group. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes, making it a versatile tool in medicinal chemistry and drug discovery.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 96.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,620.00
inventory 100mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿3,195.00
inventory 5g
10-20 days ฿9,729.00

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(S)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acid
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This chemical is primarily used as an intermediate in the synthesis of pharmaceutical compounds. It plays a crucial role in the production of various active pharmaceutical ingredients (APIs), particularly those involving piperazine derivatives. Its structure is valuable in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, it is utilized in peptide synthesis, where it helps in building complex peptide chains by providing a protected carboxylic acid group. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthetic processes, making it a versatile tool in medicinal chemistry and drug discovery.
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