(S)-tert-Butyl 5-bromo-2-((tert-butoxycarbonyl)amino)pentanoate

≥95%

Reagent Code: #38574
fingerprint
CAS Number 91229-86-6

science Other reagents with same CAS 91229-86-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.26 g/mol
Formula C₁₄H₂₆BrNO₄
badge Registry Numbers
MDL Number MFCD22576481
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in the pharmaceutical industry. It is often employed in the synthesis of peptides and peptidomimetics, where its tert-butoxycarbonyl (Boc) protecting group safeguards the amino functionality during reactions. The bromo substituent allows for further functionalization through substitution reactions, making it a versatile building block for constructing larger molecular frameworks. Its application is critical in the development of bioactive compounds, including potential drug candidates, where precise control over stereochemistry and functional group manipulation is essential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,497.00
inventory 100mg
10-20 days ฿3,744.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-tert-Butyl 5-bromo-2-((tert-butoxycarbonyl)amino)pentanoate
No image available

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in the pharmaceutical industry. It is often employed in the synthesis of peptides and peptidomimetics, where its tert-butoxycarbonyl (Boc) protecting group safeguards the amino functionality during reactions. The bromo substituent allows for further functionalization through substitution reactions, making it a versatile building block for constructing larger molecular frame

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in the pharmaceutical industry. It is often employed in the synthesis of peptides and peptidomimetics, where its tert-butoxycarbonyl (Boc) protecting group safeguards the amino functionality during reactions. The bromo substituent allows for further functionalization through substitution reactions, making it a versatile building block for constructing larger molecular frameworks. Its application is critical in the development of bioactive compounds, including potential drug candidates, where precise control over stereochemistry and functional group manipulation is essential.

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...