1-Benzhydryl-3-iodoazetidine

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Reagent Code: #145596
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CAS Number 125735-40-2

science Other reagents with same CAS 125735-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 349.21 g/mol
Formula C₁₆H₁₆IN
badge Registry Numbers
MDL Number MFCD08062427
thermostat Physical Properties
Melting Point 101-102°C
Boiling Point 377.4°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of highly selective receptor modulators, making it valuable in the research of antipsychotic and anticonvulsant drugs. The iodine moiety allows for further functionalization through cross-coupling reactions, enabling rapid diversification in drug discovery programs. Additionally, its benzhydryl group contributes to enhanced lipophilicity and blood-brain barrier penetration, which is advantageous in designing neuroactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿690.00
inventory 1g
10-20 days ฿3,120.00
inventory 5g
10-20 days ฿14,960.00
inventory 50mg
10-20 days ฿340.00

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1-Benzhydryl-3-iodoazetidine
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of highly selective receptor modulators, making it valuable in the research of antipsychotic and anticonvulsant drugs. The iodine moiety allows for further functionalization through cross-coupling reactions, enabling rapid diversification in drug discovery programs. Additionally, its benzhydryl group contributes to e

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of highly selective receptor modulators, making it valuable in the research of antipsychotic and anticonvulsant drugs. The iodine moiety allows for further functionalization through cross-coupling reactions, enabling rapid diversification in drug discovery programs. Additionally, its benzhydryl group contributes to enhanced lipophilicity and blood-brain barrier penetration, which is advantageous in designing neuroactive molecules.

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