(R)-5, 6-Difluoro-2, 3-dihydro-1H-inden-1-amine hydrochloride

95%

Reagent Code: #231076
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CAS Number 1637453-74-7

science Other reagents with same CAS 1637453-74-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.63 g/mol
Formula C₉H₁₀ClF₂N
badge Registry Numbers
MDL Number MFCD26585561
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective enzyme inhibitors and central nervous system therapeutics. Its stereochemistry enables high enantioselectivity in drug formulations, improving potency and reducing off-target effects. Commonly employed in the production of antiviral and neurodegenerative disease treatments due to its ability to cross the blood-brain barrier efficiently. Also utilized in asymmetric synthesis routes where amine functionality acts as a directing group or catalytic site.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿6,950.00
100mg
10-20 days ฿10,350.00
250mg
10-20 days ฿17,610.00
(R)-5, 6-Difluoro-2, 3-dihydro-1H-inden-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 enzyme inhibitors and central nervous system therapeutics. Its stereochemistry enables high enantioselectivity in drug formulations, improving potency and reducing off-target effects. Commonly employed in the production of antiviral and neurodegenerative disease treatments due to its ability to cross the blood-brain barrier efficiently. Also utilized in asymmetric synthesis routes whe

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective enzyme inhibitors and central nervous system therapeutics. Its stereochemistry enables high enantioselectivity in drug formulations, improving potency and reducing off-target effects. Commonly employed in the production of antiviral and neurodegenerative disease treatments due to its ability to cross the blood-brain barrier efficiently. Also utilized in asymmetric synthesis routes where amine functionality acts as a directing group or catalytic site.

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