(S)-4-Bromo-2-((tert-butoxycarbonyl)amino)pent-4-enoic acid

≥98%

Reagent Code: #38528
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CAS Number 151215-34-8

science Other reagents with same CAS 151215-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.14 g/mol
Formula C₁₀H₁₆BrNO₄
badge Registry Numbers
MDL Number MFCD01320852
thermostat Physical Properties
Boiling Point 396.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of peptide-based drugs due to its ability to introduce specific functional groups into peptide chains. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Additionally, the presence of the bromoalkene moiety makes it a versatile building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in medicinal chemistry to create diverse drug candidates. Its application is particularly valuable in the synthesis of bioactive compounds targeting various diseases.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,093.00
inventory 100mg
10-20 days ฿9,198.00
inventory 1g
10-20 days ฿26,469.00

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(S)-4-Bromo-2-((tert-butoxycarbonyl)amino)pent-4-enoic acid
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This chemical is primarily used in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of peptide-based drugs due to its ability to introduce specific functional groups into peptide chains. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. A

This chemical is primarily used in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of peptide-based drugs due to its ability to introduce specific functional groups into peptide chains. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Additionally, the presence of the bromoalkene moiety makes it a versatile building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in medicinal chemistry to create diverse drug candidates. Its application is particularly valuable in the synthesis of bioactive compounds targeting various diseases.

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