1-(tert-Butoxycarbonyl)-1,4-diazepane-5-carboxylic acid

95%

Reagent Code: #39575
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CAS Number 1214824-64-2

science Other reagents with same CAS 1214824-64-2

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Weight 244.2875 g/mol
Formula C₁₁H₂₀N₂O₄
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MDL Number MFCD09752214
inventory_2 Storage & Handling
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description Product Description

This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive molecules, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a diazepane ring, makes it valuable for constructing nitrogen-containing heterocycles, which are common in medicinal chemistry. The Boc group can be easily removed under mild conditions, allowing for further functionalization of the molecule. Additionally, its carboxylic acid moiety enables coupling reactions, facilitating the creation of peptides or other amide-linked compounds. This compound is especially relevant in the development of central nervous system (CNS) drugs, as the diazepane scaffold is often found in molecules targeting neurological pathways.

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inventory 50mg
10-20 days ฿7,317.00

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1-(tert-Butoxycarbonyl)-1,4-diazepane-5-carboxylic acid
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This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive molecules, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a diazepane ring, makes it valuable for constructing nitrogen-containing heterocycles, which are common in medicinal chemistry. The Boc group can be easily removed under mild conditio

This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive molecules, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a diazepane ring, makes it valuable for constructing nitrogen-containing heterocycles, which are common in medicinal chemistry. The Boc group can be easily removed under mild conditions, allowing for further functionalization of the molecule. Additionally, its carboxylic acid moiety enables coupling reactions, facilitating the creation of peptides or other amide-linked compounds. This compound is especially relevant in the development of central nervous system (CNS) drugs, as the diazepane scaffold is often found in molecules targeting neurological pathways.

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