(S)-(-)-Glycidol

97%

Reagent Code: #234600
label
Alias (S)-(-)-1 - hydroxy-1,3 - propylene oxide, (S)-(-)-2-(hydroxymethyl)ethylene oxide, (S)-epoxypropyl alcohol, (S)-(-)-epoxypropyl alcohol, (S)-(-)-2,3-epoxy-1-propanol, (S)-(-)-ethylene oxide-2-methanol
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CAS Number 60456-23-7

science Other reagents with same CAS 60456-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 74.08 g/mol
Formula C₃H₆O₂
badge Registry Numbers
MDL Number MFCD00074874
thermostat Physical Properties
Boiling Point 66-67 °C19 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.116 g/mL at 20 °C(lit.)
Storage -20°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in a stereocontrolled manner. Commonly employed in the preparation of optically active intermediates for drugs like propranolol and atenolol. Also utilized in the synthesis of fine chemicals, agrochemicals, and specialty polymers where enantiomeric purity is critical. Due to its reactivity, it serves as a precursor in asymmetric synthesis and is valued in research and development of new bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿900.00
inventory 25g
10-20 days ฿4,220.00

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(S)-(-)-Glycidol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its epoxide ring allows for selective ring-opening reactions, enabling the introduction of functional groups in a stereocontrolled manner. Commonly employed in the preparation of optically active intermediates for drugs like propranolol and atenolol. Also utilized in the synthesis of fine chemicals, agrochemicals, and specialty polymers where enantiomeric purity is critical. Due to its reactivity, it serves as a precursor in asymmetric synthesis and is valued in research and development of new bioactive molecules.
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