O-allyl-n-benzylcinchondinium bromide

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Reagent Code: #57506
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CAS Number 158195-40-5

science Other reagents with same CAS 158195-40-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 505.49 g/mol
Formula C₂₉H₃₃BrN₂O
thermostat Physical Properties
Melting Point 140-144 °C (dec.)
inventory_2 Storage & Handling
Storage room temperature, dry, inert gas

description Product Description

Used as a phase-transfer catalyst in organic synthesis, facilitating reactions between compounds in different phases. It enhances the efficiency of alkylation, acylation, and other nucleophilic substitution reactions. Commonly applied in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows it to stabilize intermediates and improve reaction selectivity. Also employed in asymmetric synthesis to achieve chiral induction, particularly in the synthesis of enantiomerically pure compounds. Its role in green chemistry is notable, as it reduces the need for hazardous solvents and harsh reaction conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,505.00

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O-allyl-n-benzylcinchondinium bromide
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Used as a phase-transfer catalyst in organic synthesis, facilitating reactions between compounds in different phases. It enhances the efficiency of alkylation, acylation, and other nucleophilic substitution reactions. Commonly applied in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows it to stabilize intermediates and improve reaction selectivity. Also employed in asymmetric synthesis to achieve chiral induction, particularly in the synthesis of enantiome

Used as a phase-transfer catalyst in organic synthesis, facilitating reactions between compounds in different phases. It enhances the efficiency of alkylation, acylation, and other nucleophilic substitution reactions. Commonly applied in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows it to stabilize intermediates and improve reaction selectivity. Also employed in asymmetric synthesis to achieve chiral induction, particularly in the synthesis of enantiomerically pure compounds. Its role in green chemistry is notable, as it reduces the need for hazardous solvents and harsh reaction conditions.

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