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

96%

Reagent Code: #231920
fingerprint
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
badge Registry Numbers
MDL Number MFCD09256234
inventory_2 Storage & Handling
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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,480.00
250mg
10-20 days ฿20,790.00
1g
10-20 days ฿51,040.00
(R)-6-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine
No image available

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.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...