(S,E)-ethyl5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoate

96%

Reagent Code: #237776
fingerprint
CAS Number 2131788-25-3

science Other reagents with same CAS 2131788-25-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.52 g/mol
Formula C₂₅H₃₁NO₄
badge Registry Numbers
MDL Number MFCD28386958
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting protease enzymes. Its structure supports peptide mimicry, making it valuable in designing inhibitors for viral or metabolic diseases. The tert-butoxycarbonyl (Boc) protecting group allows for controlled stepwise synthesis in complex molecule assembly, while the ethyl ester moiety can be hydrolyzed to introduce carboxylic acid functionality for further derivatization. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical and functional group versatility.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,910.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S,E)-ethyl5-([1,1'-biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoate
No image available

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting protease enzymes. Its structure supports peptide mimicry, making it valuable in designing inhibitors for viral or metabolic diseases. The tert-butoxycarbonyl (Boc) protecting group allows for controlled stepwise synthesis in complex molecule assembly, while the ethyl ester moiety can be hydrolyzed to introduce carboxylic acid functionality for further derivatization. Com

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting protease enzymes. Its structure supports peptide mimicry, making it valuable in designing inhibitors for viral or metabolic diseases. The tert-butoxycarbonyl (Boc) protecting group allows for controlled stepwise synthesis in complex molecule assembly, while the ethyl ester moiety can be hydrolyzed to introduce carboxylic acid functionality for further derivatization. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical and functional group versatility.

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...