(trans-2-(o-tolyl)cyclopropyl)methanol

95%

Reagent Code: #242116
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CAS Number 1391636-49-9

science Other reagents with same CAS 1391636-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.23 g/mol
Formula C₁₁H₁₄O
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its cyclopropyl structure with a hydroxyl group enables selective functionalization, making it valuable in constructing chiral building blocks for drug design. It is often employed in the preparation of analogs for central nervous system agents and anti-inflammatory compounds. The presence of the o-tolyl group enhances steric and electronic properties useful in asymmetric synthesis. Its trans configuration is critical for achieving desired stereochemistry in final active molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,480.00
inventory 250mg
10-20 days ฿9,360.00

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(trans-2-(o-tolyl)cyclopropyl)methanol
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Used primarily as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its cyclopropyl structure with a hydroxyl group enables selective functionalization, making it valuable in constructing chiral building blocks for drug design. It is often employed in the preparation of analogs for central nervous system agents and anti-inflammatory compounds. The presence of the o-tolyl group enhances steric and electronic properties useful in asymm

Used primarily as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its cyclopropyl structure with a hydroxyl group enables selective functionalization, making it valuable in constructing chiral building blocks for drug design. It is often employed in the preparation of analogs for central nervous system agents and anti-inflammatory compounds. The presence of the o-tolyl group enhances steric and electronic properties useful in asymmetric synthesis. Its trans configuration is critical for achieving desired stereochemistry in final active molecules.

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