(S)-benzyl tert-butyl (4-hydroxybutane-1,3-diyl)dicarbamate

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Reagent Code: #84863
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CAS Number 197892-14-1

science Other reagents with same CAS 197892-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.40 g/mol
Formula C₁₇H₂₆N₂O₅
badge Registry Numbers
MDL Number MFCD22381071
thermostat Physical Properties
Boiling Point 532.7±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.153±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the production of complex molecules and pharmaceuticals. It serves as a key intermediate in the synthesis of biologically active compounds, including peptide-based drugs. Its structure, featuring both benzyl and tert-butyl protecting groups, makes it valuable for selective deprotection strategies during multi-step synthetic processes. This allows for precise control over the assembly of target molecules, especially in the development of therapeutic agents. Additionally, its chiral center (S-configuration) is crucial for synthesizing enantiomerically pure compounds, which are often required in drug development to ensure efficacy and reduce side effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,400.00
inventory 250mg
10-20 days ฿9,450.00
inventory 1g
10-20 days ฿18,900.00

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(S)-benzyl tert-butyl (4-hydroxybutane-1,3-diyl)dicarbamate
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This chemical is primarily utilized in the field of organic synthesis, particularly in the production of complex molecules and pharmaceuticals. It serves as a key intermediate in the synthesis of biologically active compounds, including peptide-based drugs. Its structure, featuring both benzyl and tert-butyl protecting groups, makes it valuable for selective deprotection strategies during multi-step synthetic processes. This allows for precise control over the assembly of target molecules, especially in

This chemical is primarily utilized in the field of organic synthesis, particularly in the production of complex molecules and pharmaceuticals. It serves as a key intermediate in the synthesis of biologically active compounds, including peptide-based drugs. Its structure, featuring both benzyl and tert-butyl protecting groups, makes it valuable for selective deprotection strategies during multi-step synthetic processes. This allows for precise control over the assembly of target molecules, especially in the development of therapeutic agents. Additionally, its chiral center (S-configuration) is crucial for synthesizing enantiomerically pure compounds, which are often required in drug development to ensure efficacy and reduce side effects.

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