(S)-1-Cyclopropylethan-1-ol

98%

Reagent Code: #233056
label
Alias 1-cyclopropylethanol; (1S)-1-cyclopropylethane-1-ol; 1-cyclopropylethanol; (S)-1-cyclopropylethanol
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CAS Number 55637-37-1

science Other reagents with same CAS 55637-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 86.13 g/mol
Formula C₅H₁₀O
badge Registry Numbers
MDL Number MFCD08702991
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its cyclopropyl and hydroxyl functional groups allow for selective transformations in multi-step organic syntheses. Commonly employed in the preparation of antiviral and anticancer agents, as well as in the manufacture of agrochemicals requiring enantiomerically pure intermediates. The compound’s structural rigidity from the cyclopropane ring enhances selectivity in drug design.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿16,450.00
inventory 100mg
10-20 days ฿28,560.00
inventory 1g
10-20 days ฿134,480.00
inventory 250mg
10-20 days ฿48,110.00
(S)-1-Cyclopropylethan-1-ol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its cyclopropyl and hydroxyl functional groups allow for selective transformations in multi-step organic syntheses. Commonly employed in the preparation of antiviral and anticancer agents, as well as in the manufacture of agrochemicals requiring enantiomerically pure intermediates. The compound’

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its cyclopropyl and hydroxyl functional groups allow for selective transformations in multi-step organic syntheses. Commonly employed in the preparation of antiviral and anticancer agents, as well as in the manufacture of agrochemicals requiring enantiomerically pure intermediates. The compound’s structural rigidity from the cyclopropane ring enhances selectivity in drug design.

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