tert-Butyl (4-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)butyl)carbamate

98%

Reagent Code: #233191
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CAS Number 1001575-89-8

science Other reagents with same CAS 1001575-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 414.56 g/mol
Formula C₁₉H₃₄N₄O₄S
thermostat Physical Properties
Melting Point 178-180 °C
Boiling Point 709.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.136±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

This biotin derivative, featuring a stereospecific (3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl moiety linked via a pentanamido-butyl chain to a tert-butyloxycarbonyl (Boc)-protected amine, serves as a versatile protected intermediate in bioconjugation and pharmaceutical research. It is particularly valuable for synthesizing biotinylated peptides, proteins, and therapeutics, enabling specific targeting through the high-affinity avidin-biotin interaction. The Boc group facilitates incorporation into complex molecules via solid-phase or solution-phase synthesis, with easy deprotection for further modifications. Applications include affinity purification, immunoassay development (e.g., ELISA), enzyme inhibitor design, receptor ligand preparation, and targeted drug delivery systems where precise stereochemistry ensures biological specificity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿20,140.00
inventory 100mg
10-20 days ฿32,210.00
tert-Butyl (4-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)butyl)carbamate
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This biotin derivative, featuring a stereospecific (3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl moiety linked via a pentanamido-butyl chain to a tert-butyloxycarbonyl (Boc)-protected amine, serves as a versatile protected intermediate in bioconjugation and pharmaceutical research. It is particularly valuable for synthesizing biotinylated peptides, proteins, and therapeutics, enabling specific targeting through the high-affinity avidin-biotin interaction. The Boc group facilitates incorporati

This biotin derivative, featuring a stereospecific (3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl moiety linked via a pentanamido-butyl chain to a tert-butyloxycarbonyl (Boc)-protected amine, serves as a versatile protected intermediate in bioconjugation and pharmaceutical research. It is particularly valuable for synthesizing biotinylated peptides, proteins, and therapeutics, enabling specific targeting through the high-affinity avidin-biotin interaction. The Boc group facilitates incorporation into complex molecules via solid-phase or solution-phase synthesis, with easy deprotection for further modifications. Applications include affinity purification, immunoassay development (e.g., ELISA), enzyme inhibitor design, receptor ligand preparation, and targeted drug delivery systems where precise stereochemistry ensures biological specificity.

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