4-((tert-Butoxycarbonyl)amino)-2-chlorobenzoic acid

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Reagent Code: #46052
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CAS Number 232275-73-9

science Other reagents with same CAS 232275-73-9

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Weight 271.7000 g/mol
Formula C₁₂H₁₄ClNO₄
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MDL Number MFCD02682164
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This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic effects. The tert-butoxycarbonyl (Boc) protecting group is crucial in peptide synthesis, where it safeguards the amino group during reactions, allowing selective modifications to other parts of the molecule. Additionally, its chlorobenzoic acid moiety makes it a versatile intermediate for further functionalization, such as coupling reactions or the creation of heterocyclic structures. Its applications extend to material science, where it can be used to design specialized polymers or coatings with tailored properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,222.00

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4-((tert-Butoxycarbonyl)amino)-2-chlorobenzoic acid
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This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic effects. The tert-butoxycarbonyl (Boc) protecting group is crucial in peptide synthesis, where it safeguards the amino group during reactions, allowing selective modifications to other parts of the

This compound is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic effects. The tert-butoxycarbonyl (Boc) protecting group is crucial in peptide synthesis, where it safeguards the amino group during reactions, allowing selective modifications to other parts of the molecule. Additionally, its chlorobenzoic acid moiety makes it a versatile intermediate for further functionalization, such as coupling reactions or the creation of heterocyclic structures. Its applications extend to material science, where it can be used to design specialized polymers or coatings with tailored properties.

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