(S)-1,3-Dihydrospiro[indene-2,4'-piperidin]-1-amine dihydrochloride

98%

Reagent Code: #236004
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CAS Number 2306254-23-7

science Other reagents with same CAS 2306254-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.22 g/mol
Formula C₁₃H₂₀Cl₂N₂
badge Registry Numbers
MDL Number MFCD32068285
inventory_2 Storage & Handling
Storage Room temperature, airtight, 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 receptor modulators. Its spirocyclic structure and amine functionality make it valuable in medicinal chemistry for constructing bioactive molecules with high enantioselectivity. Commonly employed in the preparation of central nervous system (CNS) active compounds due to its ability to cross the blood-brain barrier and interact with neurological targets. Also utilized in research settings for structure-activity relationship (SAR) studies involving piperidine-based analogs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿930.00
inventory 250mg
10-20 days ฿1,760.00
inventory 1g
10-20 days ฿6,400.00
inventory 5g
10-20 days ฿28,800.00
inventory 10g
10-20 days ฿56,000.00
inventory 25g
10-20 days ฿136,000.00

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(S)-1,3-Dihydrospiro[indene-2,4'-piperidin]-1-amine dihydrochloride
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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 receptor modulators. Its spirocyclic structure and amine functionality make it valuable in medicinal chemistry for constructing bioactive molecules with high enantioselectivity. Commonly employed in the preparation of central nervous system (CNS) active compounds due to its ability to cross the blood-brain barrier and interact with neurological targets. Also util

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective enzyme inhibitors and receptor modulators. Its spirocyclic structure and amine functionality make it valuable in medicinal chemistry for constructing bioactive molecules with high enantioselectivity. Commonly employed in the preparation of central nervous system (CNS) active compounds due to its ability to cross the blood-brain barrier and interact with neurological targets. Also utilized in research settings for structure-activity relationship (SAR) studies involving piperidine-based analogs.

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