(1R)-1-(4-FLUOROPHENYL)-2-METHYLPROPYLAMINE-HCl

95%

Reagent Code: #230211
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CAS Number 1213329-40-8

science Other reagents with same CAS 1213329-40-8

blur_circular Chemical Specifications

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Weight 203.68 g/mol
Formula C₁₀H₁₅ClFN
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Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of central nervous system agents and other bioactive molecules where stereochemistry plays a critical role in efficacy. Commonly employed in asymmetric synthesis routes due to its stable amine functionality and fluorinated aromatic motif, which enhances binding affinity in drug-receptor interactions. Widely utilized in research and development for novel therapeutic compounds, especially in the area of neurodegenerative and psychiatric disorders. Due to its structural similarity to amphetamine derivatives, it must be handled with caution and is subject to strict regulatory controls to prevent misuse as a precursor for controlled substances.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,860.00
inventory 250mg
10-20 days ฿11,160.00
inventory 1g
10-20 days ฿27,820.00

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(1R)-1-(4-FLUOROPHENYL)-2-METHYLPROPYLAMINE-HCl
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of central nervous system agents and other bioactive molecules where stereochemistry plays a critical role in efficacy. Commonly employed in asymmetric synthesis routes due to its stable amine functionality and fluorinated aromatic motif, which enhances binding affinity in drug-receptor inte

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the development of central nervous system agents and other bioactive molecules where stereochemistry plays a critical role in efficacy. Commonly employed in asymmetric synthesis routes due to its stable amine functionality and fluorinated aromatic motif, which enhances binding affinity in drug-receptor interactions. Widely utilized in research and development for novel therapeutic compounds, especially in the area of neurodegenerative and psychiatric disorders. Due to its structural similarity to amphetamine derivatives, it must be handled with caution and is subject to strict regulatory controls to prevent misuse as a precursor for controlled substances.

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