4-((tert-Butoxycarbonyl)amino)-1-methylcyclohexanecarboxylic acid

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Reagent Code: #124240
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CAS Number 1262406-79-0

science Other reagents with same CAS 1262406-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.33 g/mol
Formula C₁₃H₂₃NO₄
badge Registry Numbers
MDL Number MFCD18374849
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is valuable in peptide synthesis, where it safeguards the amino group during reactions, allowing selective deprotection later. The compound’s structure, featuring a carboxylic acid and a protected amine, makes it versatile for constructing complex molecules, such as drug candidates targeting neurological or metabolic disorders. Additionally, it can be utilized in the preparation of cyclohexane-based scaffolds, which are common in medicinal chemistry for their conformational stability and potential therapeutic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿46,800.00
inventory 100mg
10-20 days ฿13,374.00
inventory 250mg
10-20 days ฿23,400.00

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4-((tert-Butoxycarbonyl)amino)-1-methylcyclohexanecarboxylic acid
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This compound is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is valuable in peptide synthesis, where it safeguards the amino group during reactions, allowing selective deprotection later. The compound’s structure, featuring a carboxylic acid and a protected amine, makes it versatile for constructing complex molecules, such as drug candidates targeting neurological or meta

This compound is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its tert-butoxycarbonyl (Boc) protecting group is valuable in peptide synthesis, where it safeguards the amino group during reactions, allowing selective deprotection later. The compound’s structure, featuring a carboxylic acid and a protected amine, makes it versatile for constructing complex molecules, such as drug candidates targeting neurological or metabolic disorders. Additionally, it can be utilized in the preparation of cyclohexane-based scaffolds, which are common in medicinal chemistry for their conformational stability and potential therapeutic applications.

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