(R)-5-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride

97%

Reagent Code: #230494
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CAS Number 1443238-61-6

science Other reagents with same CAS 1443238-61-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.55 g/mol
Formula C₉H₁₁BrClN
badge Registry Numbers
MDL Number MFCD29042773
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its enantiomerically pure amine group allows for selective interactions in drug design, making it valuable in creating serotonin and dopamine receptor modulators. Commonly employed in asymmetric synthesis to introduce stereochemistry in complex molecules. Also utilized in the preparation of intermediates for neurodegenerative disease treatments, including Parkinson’s and Alzheimer’s research. Its rigid indane scaffold enhances binding specificity and metabolic stability in active compounds.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to gray to yellow powder or crystals
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,105.50
inventory 250mg
10-20 days ฿1,677.50
inventory 1g
10-20 days ฿11,530.00
(R)-5-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its enantiomerically pure amine group allows for selective interactions in drug design, making it valuable in creating serotonin and dopamine receptor modulators. Commonly employed in asymmetric synthesis to introduce stereochemistry in complex molecules. Also utilized in the preparation of intermediates for neurodegenerative disease treatments, including Parkinson’s and

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its enantiomerically pure amine group allows for selective interactions in drug design, making it valuable in creating serotonin and dopamine receptor modulators. Commonly employed in asymmetric synthesis to introduce stereochemistry in complex molecules. Also utilized in the preparation of intermediates for neurodegenerative disease treatments, including Parkinson’s and Alzheimer’s research. Its rigid indane scaffold enhances binding specificity and metabolic stability in active compounds.

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