(R)-6-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine

96%

Reagent Code: #231920
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CAS Number 1213003-24-7

science Other reagents with same CAS 1213003-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.11 g/mol
Formula C₁₀H₁₂BrN
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MDL Number MFCD09256234
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Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its stereochemistry plays a critical role in ensuring high enantiomeric purity of the final drug product, which can significantly influence efficacy and reduce side effects. Commonly employed in asymmetric synthesis routes where the (R)-configuration is essential for biological activity. Also utilized in the preparation of β-adrenergic receptor modulators and dopaminergic agents. Its amine functionality allows for easy derivatization, making it valuable in medicinal chemistry for constructing complex drug molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,480.00
inventory 250mg
10-20 days ฿20,790.00
inventory 1g
10-20 days ฿51,040.00

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(R)-6-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its stereochemistry plays a critical role in ensuring high enantiomeric purity of the final drug product, which can significantly influence efficacy and reduce side effects. Commonly employed in asymmetric synthesis routes where the (R)-configuration is essential for biological activity. Als

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active compounds. Its stereochemistry plays a critical role in ensuring high enantiomeric purity of the final drug product, which can significantly influence efficacy and reduce side effects. Commonly employed in asymmetric synthesis routes where the (R)-configuration is essential for biological activity. Also utilized in the preparation of β-adrenergic receptor modulators and dopaminergic agents. Its amine functionality allows for easy derivatization, making it valuable in medicinal chemistry for constructing complex drug molecules.

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