tert-Butyl (trans-3-hydroxy-2,2,4,4-tetramethylcyclobutyl)carbamate

97%

Reagent Code: #83030
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CAS Number 1338812-41-1

science Other reagents with same CAS 1338812-41-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.34 g/mol
Formula C₁₃H₂₅NO₃
badge Registry Numbers
MDL Number MFCD20923769
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring a cyclobutyl ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in pharmaceutical research. It is often employed in the development of drugs targeting neurological disorders, as the cyclobutyl moiety can enhance binding affinity to specific receptors. Additionally, its stability and reactivity make it suitable for use in peptide synthesis, where it can act as a protecting group for amines, ensuring selective reactions during the assembly of peptide chains.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,667.00

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tert-Butyl (trans-3-hydroxy-2,2,4,4-tetramethylcyclobutyl)carbamate
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring a cyclobutyl ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in pharmaceutical research. It is often employed in the development of drugs targeting neurological disorders, as the cyclobutyl moiety can enhance binding affinity to specific receptors. Additionall

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring a cyclobutyl ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in pharmaceutical research. It is often employed in the development of drugs targeting neurological disorders, as the cyclobutyl moiety can enhance binding affinity to specific receptors. Additionally, its stability and reactivity make it suitable for use in peptide synthesis, where it can act as a protecting group for amines, ensuring selective reactions during the assembly of peptide chains.

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