1-(2-(4-Methoxyphenyl)cyclopropyl)ethan-1-one

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Reagent Code: #213556
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CAS Number 54064-36-7

science Other reagents with same CAS 54064-36-7

blur_circular Chemical Specifications

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Weight 190.24 g/mol
Formula C₁₂H₁₄O₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its cyclopropyl structure with a ketone and methoxyaryl group makes it valuable in developing analogs for drug discovery, particularly in central nervous system agents and anti-inflammatory compounds. Commonly employed in cross-coupling reactions and ring-expansion transformations to build complex molecular architectures. Also utilized in the preparation of chiral building blocks due to the rigidity of the cyclopropane ring, which can influence stereoselectivity in downstream reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,300.00

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1-(2-(4-Methoxyphenyl)cyclopropyl)ethan-1-one
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its cyclopropyl structure with a ketone and methoxyaryl group makes it valuable in developing analogs for drug discovery, particularly in central nervous system agents and anti-inflammatory compounds. Commonly employed in cross-coupling reactions and ring-expansion transformations to build complex molecular architectures. Also utilized in the preparation of chiral building blocks due to the rigidity of the cycloprop

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its cyclopropyl structure with a ketone and methoxyaryl group makes it valuable in developing analogs for drug discovery, particularly in central nervous system agents and anti-inflammatory compounds. Commonly employed in cross-coupling reactions and ring-expansion transformations to build complex molecular architectures. Also utilized in the preparation of chiral building blocks due to the rigidity of the cyclopropane ring, which can influence stereoselectivity in downstream reactions.

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