(R)-1-(3-Methoxyphenyl)propan-1-amine

95%

Reagent Code: #230871
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CAS Number 623143-36-2

science Other reagents with same CAS 623143-36-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.23 g/mol
Formula C₁₀H₁₅NO
badge Registry Numbers
MDL Number MFCD08057311
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system (CNS) active compounds. Its enantiomeric purity makes it valuable in developing drugs with selective biological activity, including antidepressants and anti-anxiety agents. Also employed in the preparation of beta-3 adrenergic receptor agonists for metabolic and urinary disorders. Commonly utilized in asymmetric synthesis due to its stable amine functionality and aromatic moiety, facilitating carbon-carbon bond formation in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿39,890.00

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(R)-1-(3-Methoxyphenyl)propan-1-amine
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system (CNS) active compounds. Its enantiomeric purity makes it valuable in developing drugs with selective biological activity, including antidepressants and anti-anxiety agents. Also employed in the preparation of beta-3 adrenergic receptor agonists for metabolic and urinary disorders. Commonly utilized in asymmetric synthesis due to its stable amine functionality and aromatic moiety, facil
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of central nervous system (CNS) active compounds. Its enantiomeric purity makes it valuable in developing drugs with selective biological activity, including antidepressants and anti-anxiety agents. Also employed in the preparation of beta-3 adrenergic receptor agonists for metabolic and urinary disorders. Commonly utilized in asymmetric synthesis due to its stable amine functionality and aromatic moiety, facilitating carbon-carbon bond formation in medicinal chemistry research.
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