2-(4-Isopropylphenyl)Ethanamine

95%

Reagent Code: #200640
fingerprint
CAS Number 84558-03-2

science Other reagents with same CAS 84558-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.26 g/mol
Formula C₁₁H₁₇N
badge Registry Numbers
MDL Number MFCD06212662
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a specialty chemical intermediate in the synthesis of pharmaceuticals, particularly for developing compounds with central nervous system (CNS) activity, such as certain antidepressants, stimulants, and analgesics. Its phenethylamine scaffold supports the creation of bioactive derivatives that interact with neurotransmitter systems. Note: Not directly associated with ibuprofen or traditional NSAIDs, but useful in related aryl-substituted analogs. Also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, enhancing the efficiency and selectivity of organic reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,260.00
inventory 1g
10-20 days ฿5,690.00
inventory 5g
10-20 days ฿19,800.00
2-(4-Isopropylphenyl)Ethanamine
No image available

Used as a specialty chemical intermediate in the synthesis of pharmaceuticals, particularly for developing compounds with central nervous system (CNS) activity, such as certain antidepressants, stimulants, and analgesics. Its phenethylamine scaffold supports the creation of bioactive derivatives that interact with neurotransmitter systems. Note: Not directly associated with ibuprofen or traditional NSAIDs, but useful in related aryl-substituted analogs. Also employed in the preparation of chiral catalyst

Used as a specialty chemical intermediate in the synthesis of pharmaceuticals, particularly for developing compounds with central nervous system (CNS) activity, such as certain antidepressants, stimulants, and analgesics. Its phenethylamine scaffold supports the creation of bioactive derivatives that interact with neurotransmitter systems. Note: Not directly associated with ibuprofen or traditional NSAIDs, but useful in related aryl-substituted analogs. Also employed in the preparation of chiral catalysts and ligands for asymmetric synthesis, enhancing the efficiency and selectivity of organic reactions.

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...