(trans-2-(2-methoxyphenyl)cyclopropyl)methanol

96%

Reagent Code: #241794
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CAS Number 1683523-44-5

science Other reagents with same CAS 1683523-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.23 g/mol
Formula C₁₁H₁₄O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of centrally acting agents targeting neurological pathways. Its rigid cyclopropane core and functional groups make it valuable for structure-activity relationship studies in drug design. Commonly employed in the preparation of serotonin receptor modulators and other bioactive molecules where stereochemistry influences potency. Also utilized in asymmetric synthesis due to its stable chiral structure, enabling selective transformations in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,400.00
inventory 500mg
10-20 days ฿18,900.00
inventory 1g
10-20 days ฿23,400.00
inventory 100mg
10-20 days ฿5,197.50

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(trans-2-(2-methoxyphenyl)cyclopropyl)methanol
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Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of centrally acting agents targeting neurological pathways. Its rigid cyclopropane core and functional groups make it valuable for structure-activity relationship studies in drug design. Commonly employed in the preparation of serotonin receptor modulators and other bioactive molecules where stereochemistry influences potency. Also utilized in asymmetric synthesis due to its stable chiral structure, ena
Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of centrally acting agents targeting neurological pathways. Its rigid cyclopropane core and functional groups make it valuable for structure-activity relationship studies in drug design. Commonly employed in the preparation of serotonin receptor modulators and other bioactive molecules where stereochemistry influences potency. Also utilized in asymmetric synthesis due to its stable chiral structure, enabling selective transformations in multi-step synthetic routes.
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