(R)-6-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride

97%

Reagent Code: #230493
fingerprint
CAS Number 731859-02-2

science Other reagents with same CAS 731859-02-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.64 g/mol
Formula C₉H₁₁ClFN
badge Registry Numbers
MDL Number MFCD16295032
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective norepinephrine reuptake inhibitors. Its enantiomeric purity is critical for optimal biological activity in central nervous system therapeutics. Commonly employed in the development of antidepressants and anxiolytic drugs due to its role in enhancing neurotransmitter regulation. Also utilized in asymmetric synthesis routes where stereochemical control is essential for drug efficacy and safety.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,850.00
inventory 250mg
10-20 days ฿8,600.00
inventory 1g
10-20 days ฿26,600.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-6-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride
No image available

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective norepinephrine reuptake inhibitors. Its enantiomeric purity is critical for optimal biological activity in central nervous system therapeutics. Commonly employed in the development of antidepressants and anxiolytic drugs due to its role in enhancing neurotransmitter regulation. Also utilized in asymmetric synthesis routes where stereochemical control is essential for drug efficacy and

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective norepinephrine reuptake inhibitors. Its enantiomeric purity is critical for optimal biological activity in central nervous system therapeutics. Commonly employed in the development of antidepressants and anxiolytic drugs due to its role in enhancing neurotransmitter regulation. Also utilized in asymmetric synthesis routes where stereochemical control is essential for drug efficacy and safety.

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...