tert-Butyl 2,2,2-trichloroacetimidate

97%

Reagent Code: #122377
label
Alias tert-Butyl 2,2,2-trichloroimidoacetate tert-butyl trichloroacetimidate
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CAS Number 98946-18-0

science Other reagents with same CAS 98946-18-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.51 g/mol
Formula C₆H₁₀Cl₃NO
badge Registry Numbers
MDL Number MFCD00077410
thermostat Physical Properties
Melting Point 21 °C(lit.)
Boiling Point 65 °C11 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.222
Storage 2~8°C

description Product Description

This chemical is primarily used in organic synthesis as a reagent for the introduction of the tert-butoxycarbonyl (Boc) protecting group. It is particularly valuable in peptide synthesis, where it helps protect amine groups during the formation of peptide bonds, preventing unwanted side reactions. Additionally, it is employed in the preparation of glycosyl donors for carbohydrate chemistry, facilitating the synthesis of complex sugars. Its reactivity and stability make it a useful tool in the development of pharmaceuticals and fine chemicals.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 97-100
Purity (Titration by AgNO3 after O2 Combustion) 96.5-103.5
Purity (Titration by AgNO3 after O2 Combustion) 96.5-103.5
Refractive Index (N20/D) 1.454-1.458
Specific Gravity (20/20°C) 1.218-1.224
Appearance Colorless to pale yellow liquid or solid
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms To Structure
Note This product is a low melting point solid and may change state (solid, liquid, or semi-solid) in different environments.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 100g
10-20 days ฿7,480.00
inventory 5g
10-20 days ฿510.00
inventory 25g
10-20 days ฿1,930.00

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tert-Butyl 2,2,2-trichloroacetimidate
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This chemical is primarily used in organic synthesis as a reagent for the introduction of the tert-butoxycarbonyl (Boc) protecting group. It is particularly valuable in peptide synthesis, where it helps protect amine groups during the formation of peptide bonds, preventing unwanted side reactions. Additionally, it is employed in the preparation of glycosyl donors for carbohydrate chemistry, facilitating the synthesis of complex sugars. Its reactivity and stability make it a useful tool in the development

This chemical is primarily used in organic synthesis as a reagent for the introduction of the tert-butoxycarbonyl (Boc) protecting group. It is particularly valuable in peptide synthesis, where it helps protect amine groups during the formation of peptide bonds, preventing unwanted side reactions. Additionally, it is employed in the preparation of glycosyl donors for carbohydrate chemistry, facilitating the synthesis of complex sugars. Its reactivity and stability make it a useful tool in the development of pharmaceuticals and fine chemicals.

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