2-((tert-Butoxycarbonyl)amino)hex-5-enoic acid

95%

Reagent Code: #104732
fingerprint
CAS Number 214206-61-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
badge Registry Numbers
MDL Number MFCD11505911
thermostat Physical Properties
Boiling Point 369.1±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.078±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily used in organic synthesis, particularly in peptide chemistry, where it serves as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino functionality, allowing selective reactions to occur at other sites of the molecule without interference. The presence of the hex-5-enoic acid moiety makes it a versatile building block for constructing more complex molecules, especially in the synthesis of peptides and peptidomimetics. Additionally, its alkene group provides a reactive handle for further functionalization, such as through olefin metathesis or hydrofunctionalization reactions, enabling the creation of diverse molecular architectures. This compound is valuable in drug discovery and development, where precise control over molecular structure is critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,500.00
inventory 1g
10-20 days ฿29,700.00
inventory 100mg
10-20 days ฿7,200.00
2-((tert-Butoxycarbonyl)amino)hex-5-enoic acid
This compound is primarily used in organic synthesis, particularly in peptide chemistry, where it serves as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino functionality, allowing selective reactions to occur at other sites of the molecule without interference. The presence of the hex-5-enoic acid moiety makes it a versatile building block for constructing more complex molecules, especially in the synthesis of peptides and peptidomimetics. Additionally, its alkene group provides a reactive handle for further functionalization, such as through olefin metathesis or hydrofunctionalization reactions, enabling the creation of diverse molecular architectures. This compound is valuable in drug discovery and development, where precise control over molecular structure is critical.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...

Cart

No products

Subtotal: ฿0.00
Total ฿0.00 THB