(R)-8-Bromochroman-4-amine hydrochloride

≥95%

Reagent Code: #230521
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CAS Number 1810074-69-1

science Other reagents with same CAS 1810074-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.55 g/mol
Formula C₉H₁₁BrClNO
badge Registry Numbers
MDL Number MFCD24436022
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as serotonin receptor modulators. Its stereochemistry enables selective interactions in neuropharmacological targets, making it valuable in the preparation of active ingredients for antidepressants and anxiolytic drugs. Also employed in medicinal chemistry research for structure-activity relationship studies due to the bromine handle allowing further functionalization via cross-coupling reactions. The hydrochloride salt form enhances stability and water solubility, facilitating use in various reaction conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,600.00
250mg
10-20 days ฿16,470.00
(R)-8-Bromochroman-4-amine hydrochloride
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as serotonin receptor modulators. Its stereochemistry enables selective interactions in neuropharmacological targets, making it valuable in the preparation of active ingredients for antidepressants and anxiolytic drugs. Also employed in medicinal chemistry research for structure-activity relationship studies due to the bromine handle allowing further functionalization via cro

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as serotonin receptor modulators. Its stereochemistry enables selective interactions in neuropharmacological targets, making it valuable in the preparation of active ingredients for antidepressants and anxiolytic drugs. Also employed in medicinal chemistry research for structure-activity relationship studies due to the bromine handle allowing further functionalization via cross-coupling reactions. The hydrochloride salt form enhances stability and water solubility, facilitating use in various reaction conditions.

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