(S)-2-Amino-2-(3,5-dibromophenyl)ethan-1-ol hydrochloride

95%

Reagent Code: #233251
fingerprint
CAS Number 2703746-43-2

science Other reagents with same CAS 2703746-43-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.43 g/mol
Formula C₈H₁₀Br₂ClNO
badge Registry Numbers
MDL Number MFCD18376111
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents and receptor modulators. Its structural features, including the brominated aromatic ring and chiral amino alcohol core, make it valuable in asymmetric synthesis and for constructing bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the halogen atoms that can influence binding affinity and metabolic stability. Also utilized in the preparation of enzyme inhibitors and neuroactive compounds where stereochemistry plays a critical role in biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,050.00
inventory 250mg
10-20 days ฿33,020.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-2-Amino-2-(3,5-dibromophenyl)ethan-1-ol hydrochloride
No image available

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents and receptor modulators. Its structural features, including the brominated aromatic ring and chiral amino alcohol core, make it valuable in asymmetric synthesis and for constructing bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the halogen atoms that can influence binding affinity and metabolic

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents and receptor modulators. Its structural features, including the brominated aromatic ring and chiral amino alcohol core, make it valuable in asymmetric synthesis and for constructing bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the halogen atoms that can influence binding affinity and metabolic stability. Also utilized in the preparation of enzyme inhibitors and neuroactive compounds where stereochemistry plays a critical role in biological activity.

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...