(R)-1-(5-Bromothiophen-2-yl)ethan-1-aminehydrochloride

95%

Reagent Code: #231875
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CAS Number 1807938-01-7

science Other reagents with same CAS 1807938-01-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.56 g/mol
Formula C₆H₉BrClNS
badge Registry Numbers
MDL Number MFCD12760097
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its brominated thiophene ring enables further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating structurally diverse compounds. The chiral amine moiety allows for stereoselective interactions in drug targets, enhancing potency and selectivity. Commonly employed in research settings for optimizing lead compounds in drug discovery programs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿22,560.00
1g
10-20 days ฿41,540.00
(R)-1-(5-Bromothiophen-2-yl)ethan-1-aminehydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its brominated thiophene ring enables further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating structurally diverse compounds. The chiral amine moiety allows for stereoselective interactions in drug targets, enhancing potency and selectivity. Commonly employed in research settings for optimi

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its brominated thiophene ring enables further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for creating structurally diverse compounds. The chiral amine moiety allows for stereoselective interactions in drug targets, enhancing potency and selectivity. Commonly employed in research settings for optimizing lead compounds in drug discovery programs.

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