N-Boc-N-methyl-3-chloro-1-propanamine

≥95%

Reagent Code: #68172
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CAS Number 114326-14-6

science Other reagents with same CAS 114326-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.70 g/mol
Formula C₉H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD09031544
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

N-Boc-N-methyl-3-chloro-1-propanamine is widely used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. Its Boc (tert-butoxycarbonyl) protecting group makes it particularly valuable in peptide synthesis, where it helps in the selective protection of amine groups during multi-step reactions. The compound is also utilized in the development of small molecule inhibitors and other therapeutic agents, often serving as a building block for more complex structures. Additionally, its chloro functional group allows for further derivatization, enabling the creation of diverse chemical entities for drug discovery and medicinal chemistry research.

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Test Parameter Specification
Appearance Colorless to yellow liquid
Purity 95-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,476.00
inventory 250mg
10-20 days ฿5,400.00

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N-Boc-N-methyl-3-chloro-1-propanamine
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N-Boc-N-methyl-3-chloro-1-propanamine is widely used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. Its Boc (tert-butoxycarbonyl) protecting group makes it particularly valuable in peptide synthesis, where it helps in the selective protection of amine groups during multi-step reactions. The compound is also utilized in the development of small molecule inhibitors and other therapeutic agents, often serving as a building block for more co

N-Boc-N-methyl-3-chloro-1-propanamine is widely used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. Its Boc (tert-butoxycarbonyl) protecting group makes it particularly valuable in peptide synthesis, where it helps in the selective protection of amine groups during multi-step reactions. The compound is also utilized in the development of small molecule inhibitors and other therapeutic agents, often serving as a building block for more complex structures. Additionally, its chloro functional group allows for further derivatization, enabling the creation of diverse chemical entities for drug discovery and medicinal chemistry research.

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