(1S)-1-(3,4-Dimethoxyphenyl)ethan-1-amine hydrochloride

≥95%

Reagent Code: #236177
fingerprint
CAS Number 906528-67-4

science Other reagents with same CAS 906528-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.69 g/mol
Formula C₁₀H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD24422996
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of bioactive molecules and central nervous system agents. Its structure supports the creation of enantiomerically pure compounds, making it valuable in drug discovery for cardiovascular and neurological conditions. Also employed as a resolving agent due to its chirality, aiding in the separation of racemic mixtures. Commonly found in research settings for designing adrenergic agonists and studying structure-activity relationships in amine-based therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿650.00
inventory 250mg
10-20 days ฿1,550.00
inventory 1g
10-20 days ฿5,880.00
(1S)-1-(3,4-Dimethoxyphenyl)ethan-1-amine hydrochloride
No image available

Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of bioactive molecules and central nervous system agents. Its structure supports the creation of enantiomerically pure compounds, making it valuable in drug discovery for cardiovascular and neurological conditions. Also employed as a resolving agent due to its chirality, aiding in the separation of racemic mixtures. Commonly found in research settings for designing adrenergic agonists and studying st

Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of bioactive molecules and central nervous system agents. Its structure supports the creation of enantiomerically pure compounds, making it valuable in drug discovery for cardiovascular and neurological conditions. Also employed as a resolving agent due to its chirality, aiding in the separation of racemic mixtures. Commonly found in research settings for designing adrenergic agonists and studying structure-activity relationships in amine-based therapeutics.

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...