(R,E)-5-([1,1'-Biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoic acid

97%

Reagent Code: #230442
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CAS Number 1012341-48-8

science Other reagents with same CAS 1012341-48-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 381.47 g/mol
Formula C₂₃H₂₇NO₄
badge Registry Numbers
MDL Number MFCD28386950
thermostat Physical Properties
Boiling Point 595.6±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral drugs. Its structure supports the creation of peptide-like molecules that can mimic natural substrates, enabling targeted inhibition of enzymes involved in viral replication. The tert-butoxycarbonyl (Boc) protecting group allows for temporary protection of the amino group, making it suitable for synthesizing peptides or complex compounds in multi-step reactions. Commonly employed in medicinal chemistry for constructing complex molecules with high stereochemical precision.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿174.00
5g
10-20 days ฿950.00
25g
10-20 days ฿4,180.00
100g
10-20 days ฿11,820.00
10g
10-20 days ฿1,780.00
(R,E)-5-([1,1'-Biphenyl]-4-yl)-4-((tert-butoxycarbonyl)amino)-2-methylpent-2-enoic acid
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Used as an intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral drugs. Its structure supports the creation of peptide-like molecules that can mimic natural substrates, enabling targeted inhibition of enzymes involved in viral replication. The tert-butoxycarbonyl (Boc) protecting group allows for temporary protection of the amino group, making it suitable for synthesizing peptides or complex compounds in multi-step reactions. Commonly employed in medicinal chemis
Used as an intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral drugs. Its structure supports the creation of peptide-like molecules that can mimic natural substrates, enabling targeted inhibition of enzymes involved in viral replication. The tert-butoxycarbonyl (Boc) protecting group allows for temporary protection of the amino group, making it suitable for synthesizing peptides or complex compounds in multi-step reactions. Commonly employed in medicinal chemistry for constructing complex molecules with high stereochemical precision.
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