(R)-1-(m-Tolyl)propan-1-amine

98%

Reagent Code: #228581
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CAS Number 1212925-87-5

science Other reagents with same CAS 1212925-87-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.69 g/mol
Formula C₁₀H₁₆ClN
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used primarily as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of central nervous system (CNS) active agents. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it serves as an intermediate in the development of antidepressants, antipsychotics, and other neurologically targeted drugs. It is also employed in the preparation of agrochemicals and fine chemicals requiring stereochemical control. Due to its amine functionality and chiral center, it participates in reductive amination and nucleophilic addition reactions, enabling the construction of complex molecular architectures in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,550.00
inventory 1g
10-20 days ฿29,950.00

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(R)-1-(m-Tolyl)propan-1-amine
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Used primarily as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of central nervous system (CNS) active agents. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it serves as an intermediate in the development of antidepressants, antipsychotics, and other neurologically targeted drugs. It is also employed in the preparation of agrochemicals and fine chemicals requiring stereochemical control. Due to its amine functionality and chiral cen

Used primarily as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of central nervous system (CNS) active agents. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it serves as an intermediate in the development of antidepressants, antipsychotics, and other neurologically targeted drugs. It is also employed in the preparation of agrochemicals and fine chemicals requiring stereochemical control. Due to its amine functionality and chiral center, it participates in reductive amination and nucleophilic addition reactions, enabling the construction of complex molecular architectures in medicinal chemistry.

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