(S)-tert-Butyl (1-((tert-butyldimethylsilyl)oxy)-3-hydroxypropan-2-yl)carbamate

≥95%

Reagent Code: #37797
fingerprint
CAS Number 185692-85-7

science Other reagents with same CAS 185692-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.49 g/mol
Formula C₁₄H₃₁NO₄Si
badge Registry Numbers
MDL Number MFCD28403204
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptides, amino acid derivatives, and other bioactive compounds where controlled reactivity and stability are essential. Additionally, its chiral center allows for stereoselective synthesis, making it useful in the production of enantiomerically pure substances. Its applications are particularly relevant in medicinal chemistry for designing drug candidates with specific biological activities.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,059.00
inventory 1g
10-20 days ฿16,380.00
inventory 250mg
10-20 days ฿6,525.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-tert-Butyl (1-((tert-butyldimethylsilyl)oxy)-3-hydroxypropan-2-yl)carbamate
No image available

This chemical is primarily utilized in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptides, amino acid derivatives, and other bioactive compounds where controlled reactivity and stability are essential. Addi

This chemical is primarily utilized in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring both tert-butyl and tert-butyldimethylsilyl protecting groups, makes it valuable for selective deprotection strategies during multi-step syntheses. It is often employed in the development of peptides, amino acid derivatives, and other bioactive compounds where controlled reactivity and stability are essential. Additionally, its chiral center allows for stereoselective synthesis, making it useful in the production of enantiomerically pure substances. Its applications are particularly relevant in medicinal chemistry for designing drug candidates with specific biological activities.

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...