Cyclohex-3-enyl-carbamic acid tert-butyl este

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Reagent Code: #124616
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CAS Number 135262-85-0

science Other reagents with same CAS 135262-85-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.27 g/mol
Formula C₁₁H₁₉NO₂
badge Registry Numbers
MDL Number MFCD11975573
thermostat Physical Properties
Melting Point 52-54 °C
Boiling Point 288.2±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.00±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as a protective group for amines. It is particularly valuable in peptide chemistry, where it safeguards the amine functionality during complex reactions, preventing unwanted side reactions. The tert-butyl ester group can be easily removed under mild acidic conditions, making it a convenient choice for temporary protection. Additionally, it is employed in the development of pharmaceuticals and bioactive molecules, where selective protection and deprotection of functional groups are critical. Its stability under various reaction conditions allows for its use in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿11,790.00
inventory 1g
10-20 days ฿9,828.00
inventory 250mg
10-20 days ฿7,704.00

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Cyclohex-3-enyl-carbamic acid tert-butyl este
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This compound is primarily utilized in organic synthesis as a protective group for amines. It is particularly valuable in peptide chemistry, where it safeguards the amine functionality during complex reactions, preventing unwanted side reactions. The tert-butyl ester group can be easily removed under mild acidic conditions, making it a convenient choice for temporary protection. Additionally, it is employed in the development of pharmaceuticals and bioactive molecules, where selective protection and depr

This compound is primarily utilized in organic synthesis as a protective group for amines. It is particularly valuable in peptide chemistry, where it safeguards the amine functionality during complex reactions, preventing unwanted side reactions. The tert-butyl ester group can be easily removed under mild acidic conditions, making it a convenient choice for temporary protection. Additionally, it is employed in the development of pharmaceuticals and bioactive molecules, where selective protection and deprotection of functional groups are critical. Its stability under various reaction conditions allows for its use in multi-step synthetic processes.

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