(S)-5-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride

≥95%

Reagent Code: #235695
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CAS Number 1810074-82-8

science Other reagents with same CAS 1810074-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.57 g/mol
Formula C₁₀H₁₃BrClN
badge Registry Numbers
MDL Number MFCD26585976
inventory_2 Storage & Handling
Storage Room temperature, dry seal

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 enantioselectivity and biological activity in final drug products. Commonly employed in asymmetric synthesis routes where the amine functionality allows for coupling reactions or ring formation. Also utilized in the preparation of bioactive molecules targeting neurological disorders due to its structural similarity to neurotransmitter analogs. Its hydrochloride salt form enhances stability and solubility, making it suitable for use in aqueous or polar reaction media during drug manufacturing.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,160.00

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(S)-5-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 enantioselectivity and biological activity in final drug products. Commonly employed in asymmetric synthesis routes where the amine functionality allows for coupling reactions or ring formation. Also utilized in the preparation of bi

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 enantioselectivity and biological activity in final drug products. Commonly employed in asymmetric synthesis routes where the amine functionality allows for coupling reactions or ring formation. Also utilized in the preparation of bioactive molecules targeting neurological disorders due to its structural similarity to neurotransmitter analogs. Its hydrochloride salt form enhances stability and solubility, making it suitable for use in aqueous or polar reaction media during drug manufacturing.

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