1-(tert-Butyl) 2-methyl (S)-aziridine-1,2-dicarboxylate

95%

Reagent Code: #38644
fingerprint
CAS Number 126496-79-5

science Other reagents with same CAS 126496-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.2200 g/mol
Formula C₉H₁₅NO₄
badge Registry Numbers
MDL Number MFCD10566310
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of complex molecules. It is often employed in the synthesis of chiral compounds due to its stereochemical properties, making it valuable in the production of pharmaceuticals and fine chemicals. The aziridine ring in the compound is reactive, allowing it to participate in ring-opening reactions, which are useful for creating amines, amino acids, and other nitrogen-containing structures. Additionally, it serves as a precursor in the development of biologically active compounds, including potential drug candidates, by enabling the introduction of functional groups in a controlled manner. Its stability and reactivity make it a useful reagent in asymmetric synthesis and medicinal chemistry research.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to Light Yellow Liquid
Purity (%) 94.5-100
Specific Rotation ([α]28/D (c = 4.3 g/100 ml, Chloroform)) (deg) -63 to -69
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,169.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-(tert-Butyl) 2-methyl (S)-aziridine-1,2-dicarboxylate
No image available

This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of complex molecules. It is often employed in the synthesis of chiral compounds due to its stereochemical properties, making it valuable in the production of pharmaceuticals and fine chemicals. The aziridine ring in the compound is reactive, allowing it to participate in ring-opening reactions, which are useful for creating amines, amino acids, and other nitrogen-containing structures. Additionally,

This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of complex molecules. It is often employed in the synthesis of chiral compounds due to its stereochemical properties, making it valuable in the production of pharmaceuticals and fine chemicals. The aziridine ring in the compound is reactive, allowing it to participate in ring-opening reactions, which are useful for creating amines, amino acids, and other nitrogen-containing structures. Additionally, it serves as a precursor in the development of biologically active compounds, including potential drug candidates, by enabling the introduction of functional groups in a controlled manner. Its stability and reactivity make it a useful reagent in asymmetric synthesis and medicinal chemistry research.

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...