(S)-(-)-1-Phenylethanol

97%

Reagent Code: #234317
label
Alias (S)-(-)-1-phenylethanol; (S)-(-)-1-phenylethanol, (s)-(+)-sec-phenylethanol, (S)-(-)-phenylethanol
fingerprint
CAS Number 1445-91-6

science Other reagents with same CAS 1445-91-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 122.16 g/mol
Formula C₈H₁₀O
badge Registry Numbers
MDL Number MFCD00064264
thermostat Physical Properties
Melting Point 9-11 °C(lit.)
Boiling Point 88-89 °C10 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.012 g/mL at 20 °C(lit.)
Storage 2~8°C

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure drugs. Commonly employed in the resolution of racemic mixtures due to its optical activity. Serves as an intermediate in the synthesis of fragrances and flavors, contributing to floral and fruity notes in perfumery. Also utilized as a solvent or chiral auxiliary in stereoselective reactions. Its enantiomeric purity makes it valuable in research and development of chiral catalysts and ligands. Additionally, used as a standard in chromatographic analysis techniques to separate structurally similar compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿340.00
inventory 25g
10-20 days ฿1,450.00
inventory 100g
10-20 days ฿4,950.00
inventory 500g
10-20 days ฿22,660.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Cart Checkout
(S)-(-)-1-Phenylethanol
No image available
Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure drugs. Commonly employed in the resolution of racemic mixtures due to its optical activity. Serves as an intermediate in the synthesis of fragrances and flavors, contributing to floral and fruity notes in perfumery. Also utilized as a solvent or chiral auxiliary in stereoselective reactions. Its enantiomeric purity makes it valuable in research and development of
Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure drugs. Commonly employed in the resolution of racemic mixtures due to its optical activity. Serves as an intermediate in the synthesis of fragrances and flavors, contributing to floral and fruity notes in perfumery. Also utilized as a solvent or chiral auxiliary in stereoselective reactions. Its enantiomeric purity makes it valuable in research and development of chiral catalysts and ligands. Additionally, used as a standard in chromatographic analysis techniques to separate structurally similar compounds.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Recommended Dosage -
Dosage (Per Day) -
Recommended Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...