(R)-2-Amino-2-(4-(trifluoromethyl)phenyl)ethanol hydrochloride

97%

Reagent Code: #229212
fingerprint
CAS Number 2829292-57-9

science Other reagents with same CAS 2829292-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.64 g/mol
Formula C₉H₁₁ClF₃NO
badge Registry Numbers
MDL Number MFCD12758188
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical synthesis as a chiral building block for developing bioactive molecules, particularly in the production of antidepressants and other central nervous system agents. Its structural features make it valuable for enhancing metabolic stability and binding affinity in drug candidates. Commonly employed in asymmetric synthesis due to the presence of both amine and alcohol functional groups in a stereochemically defined arrangement. Also utilized in the preparation of fluorinated analogs to improve pharmacokinetic properties such as membrane permeability and resistance to oxidative degradation.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿18,450.00
250mg
10-20 days ฿27,640.00
1g
10-20 days ฿69,070.00
5g
10-20 days ฿207,150.00
(R)-2-Amino-2-(4-(trifluoromethyl)phenyl)ethanol hydrochloride
No image available

Used in pharmaceutical synthesis as a chiral building block for developing bioactive molecules, particularly in the production of antidepressants and other central nervous system agents. Its structural features make it valuable for enhancing metabolic stability and binding affinity in drug candidates. Commonly employed in asymmetric synthesis due to the presence of both amine and alcohol functional groups in a stereochemically defined arrangement. Also utilized in the preparation of fluorinated analogs t

Used in pharmaceutical synthesis as a chiral building block for developing bioactive molecules, particularly in the production of antidepressants and other central nervous system agents. Its structural features make it valuable for enhancing metabolic stability and binding affinity in drug candidates. Commonly employed in asymmetric synthesis due to the presence of both amine and alcohol functional groups in a stereochemically defined arrangement. Also utilized in the preparation of fluorinated analogs to improve pharmacokinetic properties such as membrane permeability and resistance to oxidative degradation.

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...