(R)-2-(1-Amino-2,2,2-trifluoroethyl)phenol hydrochloride

95%

Reagent Code: #37470
fingerprint
CAS Number 1394822-90-2

science Other reagents with same CAS 1394822-90-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.6114 g/mol
Formula C₈H₉ClF₃NO
badge Registry Numbers
MDL Number MFCD22393680
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its chiral structure makes it valuable in creating enantiomerically pure drugs, which are critical for ensuring efficacy and reducing side effects. Additionally, it is employed in the study of enzyme inhibition and receptor binding due to its unique trifluoroethyl group, which can enhance binding affinity and metabolic stability. Researchers also explore its potential in designing drugs for central nervous system disorders, leveraging its ability to cross the blood-brain barrier.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,176.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-(1-Amino-2,2,2-trifluoroethyl)phenol hydrochloride
No image available

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its chiral structure makes it valuable in creating enantiomerically pure drugs, which are critical for ensuring efficacy and reducing side effects. Additionally, it is employed in the study of enzyme inhibition and receptor binding due to its

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its chiral structure makes it valuable in creating enantiomerically pure drugs, which are critical for ensuring efficacy and reducing side effects. Additionally, it is employed in the study of enzyme inhibition and receptor binding due to its unique trifluoroethyl group, which can enhance binding affinity and metabolic stability. Researchers also explore its potential in designing drugs for central nervous system disorders, leveraging its ability to cross the blood-brain barrier.

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...