(R)-1,1,1-TRIFLUOROBUTAN-2-AMINE

95%

Reagent Code: #232355
fingerprint
CAS Number 1131737-02-4

science Other reagents with same CAS 1131737-02-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.11 g/mol
Formula C₄H₈F₃N
badge Registry Numbers
MDL Number MFCD16817684
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients where stereochemistry plays a critical role in biological activity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for improved bioavailability and binding affinity. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system agents and anti-inflammatory compounds. Also utilized in agrochemicals for the creation of enantiomerically pure herbicides and pesticides, where the (R)-enantiomer provides superior target selectivity and environmental safety.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,840.00
(R)-1,1,1-TRIFLUOROBUTAN-2-AMINE
No image available

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients where stereochemistry plays a critical role in biological activity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for improved bioavailability and binding affinity. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system agents and anti-i

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients where stereochemistry plays a critical role in biological activity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for improved bioavailability and binding affinity. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system agents and anti-inflammatory compounds. Also utilized in agrochemicals for the creation of enantiomerically pure herbicides and pesticides, where the (R)-enantiomer provides superior target selectivity and environmental safety.

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...