(3-(Trifluoromethyl)pyrrolidin-3-yl)methanol

97%

Reagent Code: #244451
fingerprint
CAS Number 217096-40-7

science Other reagents with same CAS 217096-40-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.14 g/mol
Formula C₆H₁₀F₃NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and metabolic diseases. Its structure supports the creation of chiral building blocks for drug candidates, enhancing metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties due to the presence of the trifluoromethyl group, which improves lipophilicity and resistance to oxidative degradation. Also utilized in the preparation of enzyme inhibitors and receptor modulators, especially in projects involving fluorinated analogs for improved efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,790.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3-(Trifluoromethyl)pyrrolidin-3-yl)methanol
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and metabolic diseases. Its structure supports the creation of chiral building blocks for drug candidates, enhancing metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties due to the presence of the trifluoromethyl group, which improves lipophilicity and resistance t

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and metabolic diseases. Its structure supports the creation of chiral building blocks for drug candidates, enhancing metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties due to the presence of the trifluoromethyl group, which improves lipophilicity and resistance to oxidative degradation. Also utilized in the preparation of enzyme inhibitors and receptor modulators, especially in projects involving fluorinated analogs for improved efficacy and selectivity.

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...