(S)-()-2-Chloro-1-phenylethanol

≥98%

Reagent Code: #71072
fingerprint
CAS Number 70111-05-6

science Other reagents with same CAS 70111-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.61 g/mol
Formula C₈H₉ClO
badge Registry Numbers
MDL Number MFCD00077692
thermostat Physical Properties
Boiling Point 114°C/6mmHg(lit.)
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as an intermediate in the preparation of β-blockers, which are essential for treating cardiovascular diseases. Additionally, it is employed in asymmetric synthesis to create compounds with high optical purity. Its role in organic synthesis extends to the development of agrochemicals and fine chemicals, where stereochemical control is crucial.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to Light orange to Yellow clear liquid
Purity 98-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,080.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-()-2-Chloro-1-phenylethanol
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as an intermediate in the preparation of β-blockers, which are essential for treating cardiovascular diseases. Additionally, it is employed in asymmetric synthesis to create compounds with high optical purity. Its role in organic synthesis extends to the development of agrochemicals and fine chemicals, where stereochemical control is crucial.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as an intermediate in the preparation of β-blockers, which are essential for treating cardiovascular diseases. Additionally, it is employed in asymmetric synthesis to create compounds with high optical purity. Its role in organic synthesis extends to the development of agrochemicals and fine chemicals, where stereochemical control is crucial.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...