1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEPTANECARBOXYLIC ACID

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Reagent Code: #39852
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CAS Number 199330-56-8

science Other reagents with same CAS 199330-56-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.33 g/mol
Formula C₁₃H₂₃NO₄
thermostat Physical Properties
Boiling Point 405.6±24.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It serves as a protected form of an amino acid, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during reactions. This protection is crucial in peptide synthesis, allowing for the selective formation of peptide bonds without unwanted side reactions. Additionally, it finds application in the development of pharmaceuticals, particularly in the synthesis of cyclic peptides and other bioactive compounds. Its cycloheptane ring structure also makes it valuable in the study of ring strain and conformational analysis in organic chemistry.

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Size Availability Unit Price Quantity
inventory 0.5g
10-20 days ฿10,800.00
inventory 1g
10-20 days ฿16,200.00
inventory 5g
10-20 days ฿48,600.00

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1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEPTANECARBOXYLIC ACID
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This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It serves as a protected form of an amino acid, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during reactions. This protection is crucial in peptide synthesis, allowing for the selective formation of peptide bonds without unwanted side reactions. Additionally, it finds application in the development of pharmaceuticals, particularly in the synthesis of cyclic
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It serves as a protected form of an amino acid, where the tert-butoxycarbonyl (Boc) group safeguards the amine functionality during reactions. This protection is crucial in peptide synthesis, allowing for the selective formation of peptide bonds without unwanted side reactions. Additionally, it finds application in the development of pharmaceuticals, particularly in the synthesis of cyclic peptides and other bioactive compounds. Its cycloheptane ring structure also makes it valuable in the study of ring strain and conformational analysis in organic chemistry.
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