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

95%

Reagent Code: #231318
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CAS Number 2241594-26-1

science Other reagents with same CAS 2241594-26-1

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 enhances efficacy and reduces side effects. Commonly employed in asymmetric synthesis routes where the amine group serves as a handle for further functionalization, such as amide coupling or reductive amination. Also utilized in the preparation of bioactive molecules targeting neurological disorders, including antidepressants and anxiolytics. Its hydrochloride salt form improves stability and solubility during manufacturing processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,280.00
inventory 250mg
10-20 days ฿27,380.00
inventory 1g
10-20 days ฿88,340.00

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(R)-6-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
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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 enhances efficacy and reduces side effects. Commonly employed in asymmetric synthesis routes where the amine group serves as a handle for further functionalization, such as amide c

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 enhances efficacy and reduces side effects. Commonly employed in asymmetric synthesis routes where the amine group serves as a handle for further functionalization, such as amide coupling or reductive amination. Also utilized in the preparation of bioactive molecules targeting neurological disorders, including antidepressants and anxiolytics. Its hydrochloride salt form improves stability and solubility during manufacturing processes.

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