2-N-Cbz-2-Methylpropane-1,2-diamine hydrochloride

≥95%

Reagent Code: #115973
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CAS Number 850033-67-9

science Other reagents with same CAS 850033-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.74 g/mol
Formula C₁₂H₁₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD11112240
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as a building block for the preparation of more complex molecules. Its protected amine group (Cbz) makes it particularly useful in peptide synthesis, where selective deprotection can be achieved without affecting other functional groups. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Additionally, its structure allows for the introduction of chiral centers, making it valuable in the synthesis of enantiomerically pure substances. Its hydrochloride form ensures stability and ease of handling during chemical reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,572.00
inventory 250mg
10-20 days ฿9,135.00

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2-N-Cbz-2-Methylpropane-1,2-diamine hydrochloride
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This compound is primarily utilized in organic synthesis and pharmaceutical research as a building block for the preparation of more complex molecules. Its protected amine group (Cbz) makes it particularly useful in peptide synthesis, where selective deprotection can be achieved without affecting other functional groups. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Additionally, its structure allows for the introduction of chira

This compound is primarily utilized in organic synthesis and pharmaceutical research as a building block for the preparation of more complex molecules. Its protected amine group (Cbz) makes it particularly useful in peptide synthesis, where selective deprotection can be achieved without affecting other functional groups. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Additionally, its structure allows for the introduction of chiral centers, making it valuable in the synthesis of enantiomerically pure substances. Its hydrochloride form ensures stability and ease of handling during chemical reactions.

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