(1R,2S)-2-(3-bromophenyl)cyclopropan-1-amine hydrochloride

98%

Reagent Code: #229326
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CAS Number 1314324-03-2

science Other reagents with same CAS 1314324-03-2

blur_circular Chemical Specifications

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Weight 248.55 g/mol
Formula C₉H₁₁BrClN
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MDL Number MFCD28390250
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its cyclopropane structure with defined stereochemistry makes it valuable in developing central nervous system agents, particularly in the design of antidepressants and antipsychotics. The bromophenyl group allows for further functionalization via cross-coupling reactions, enabling rapid diversification in drug discovery programs. Frequently employed in structure-activity relationship (SAR) studies due to its rigid framework and ability to influence binding affinity and metabolic stability.

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inventory 100mg
10-20 days ฿16,960.00

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(1R,2S)-2-(3-bromophenyl)cyclopropan-1-amine hydrochloride
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Used in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its cyclopropane structure with defined stereochemistry makes it valuable in developing central nervous system agents, particularly in the design of antidepressants and antipsychotics. The bromophenyl group allows for further functionalization via cross-coupling reactions, enabling rapid diversification in drug discovery programs. Frequently employed in structure-activity relationship (SAR) stud

Used in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its cyclopropane structure with defined stereochemistry makes it valuable in developing central nervous system agents, particularly in the design of antidepressants and antipsychotics. The bromophenyl group allows for further functionalization via cross-coupling reactions, enabling rapid diversification in drug discovery programs. Frequently employed in structure-activity relationship (SAR) studies due to its rigid framework and ability to influence binding affinity and metabolic stability.

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