(R)-1-(3-Bromophenyl)ethanamine hydrochloride

98%

Reagent Code: #230951
fingerprint
CAS Number 1167414-91-6

science Other reagents with same CAS 1167414-91-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.54 g/mol
Formula C₈H₁₁BrClN
badge Registry Numbers
MDL Number MFCD12756921
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs where the (R)-enantiomer is required for optimal biological activity. Its bromo-substituted aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of central nervous system agents and receptor-targeted compounds. The hydrochloride salt form enhances stability and solubility, facilitating handling and storage in industrial processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,860.00
inventory 5g
10-20 days ฿6,930.00
inventory 25g
10-20 days ฿33,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-1-(3-Bromophenyl)ethanamine hydrochloride
No image available

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs where the (R)-enantiomer is required for optimal biological activity. Its bromo-substituted aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of central nervous system agents and receptor-targeted compounds. The hydrochloride salt form enhances stability and solub

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs where the (R)-enantiomer is required for optimal biological activity. Its bromo-substituted aromatic ring allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of central nervous system agents and receptor-targeted compounds. The hydrochloride salt form enhances stability and solubility, facilitating handling and storage in industrial processes.

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...