3-(2-Tert-Butoxycarbonylamino-Ethylcarbamoyl)-Acrylic Acid

95%

Reagent Code: #64315
fingerprint
CAS Number 215654-55-0

science Other reagents with same CAS 215654-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.27 g/mol
Formula C₁₁H₁₈N₂O₅
badge Registry Numbers
MDL Number MFCD28968002
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in the development of peptide-based molecules. It serves as a key intermediate in the preparation of modified peptides, where its functional groups allow for selective coupling reactions. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthesis, preventing unwanted side reactions. Additionally, it finds application in the creation of bioactive compounds, including potential drug candidates, due to its ability to introduce specific structural motifs. Its acrylate moiety also makes it suitable for use in polymer chemistry, where it can participate in polymerization processes to create specialized materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,150.00
inventory 100mg
10-20 days ฿3,240.00
inventory 250mg
10-20 days ฿6,075.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(2-Tert-Butoxycarbonylamino-Ethylcarbamoyl)-Acrylic Acid
No image available

This compound is primarily utilized in the field of organic synthesis, particularly in the development of peptide-based molecules. It serves as a key intermediate in the preparation of modified peptides, where its functional groups allow for selective coupling reactions. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthesis, preventing unwanted side reactions. Additionally, it finds application in the creation of bioactive compounds, including potential drug candidates, due to

This compound is primarily utilized in the field of organic synthesis, particularly in the development of peptide-based molecules. It serves as a key intermediate in the preparation of modified peptides, where its functional groups allow for selective coupling reactions. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthesis, preventing unwanted side reactions. Additionally, it finds application in the creation of bioactive compounds, including potential drug candidates, due to its ability to introduce specific structural motifs. Its acrylate moiety also makes it suitable for use in polymer chemistry, where it can participate in polymerization processes to create specialized materials.

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...