(R)-(-)-2-Chloro-1-phenylethanol

≥98%

  • Product Code: 70950
  CAS:    56751-12-3
Molecular Weight: 156.61 g./mol Molecular Formula: C₈H₉ClO
EC Number: MDL Number: MFCD00077691
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: (R)-(-)-2-Chloro-1-phenylethanol is primarily used as a chiral intermediate in the synthesis of various pharmaceuticals. Its stereochemistry makes it valuable for producing enantiomerically pure compounds, which are crucial in drug development to ensure efficacy and reduce side effects. It is often employed in the preparation of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Additionally, this compound is utilized in organic synthesis to create other chiral molecules, serving as a building block in the production of fine chemicals and active pharmaceutical ingredients (APIs). Its role in asymmetric synthesis highlights its importance in creating high-purity, biologically active compounds.
Product Specification:
Test Specification
APPEARANCE Colorless to Light orange to Yellow clear liquid
PURITY 98-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿920.00
+
-
5.000 10-20 days ฿3,680.00
+
-
25.000 10-20 days ฿10,760.00
+
-
(R)-(-)-2-Chloro-1-phenylethanol
(R)-(-)-2-Chloro-1-phenylethanol is primarily used as a chiral intermediate in the synthesis of various pharmaceuticals. Its stereochemistry makes it valuable for producing enantiomerically pure compounds, which are crucial in drug development to ensure efficacy and reduce side effects. It is often employed in the preparation of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Additionally, this compound is utilized in organic synthesis to create other chiral molecules, serving as a building block in the production of fine chemicals and active pharmaceutical ingredients (APIs). Its role in asymmetric synthesis highlights its importance in creating high-purity, biologically active compounds.
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