(R)-1-(Thiophen-2-yl)ethanamine hydrochloride

95%

Reagent Code: #87146
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CAS Number 2252246-01-6

science Other reagents with same CAS 2252246-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.67 g/mol
Formula C₆H₁₀ClNS
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MDL Number MFCD12910712
inventory_2 Storage & Handling
Storage room temperature, inert gas storage

description Product Description

Used in pharmaceutical research as a chiral building block for the synthesis of active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting the central nervous system due to its structural similarity to certain neurotransmitters.

In organic chemistry, it serves as a precursor for the preparation of complex molecules, especially in asymmetric synthesis, where its chiral nature is exploited to induce stereoselectivity in reactions.

Additionally, it is employed in the study of enzyme mechanisms and receptor binding, aiding in the design of more effective and selective therapeutic agents. Its thiophene moiety makes it a useful intermediate in the development of compounds with potential anti-inflammatory or antimicrobial properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,613.00
inventory 1g
10-20 days ฿21,519.00
inventory 100mg
10-20 days ฿5,742.00

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(R)-1-(Thiophen-2-yl)ethanamine hydrochloride
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Used in pharmaceutical research as a chiral building block for the synthesis of active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting the central nervous system due to its structural similarity to certain neurotransmitters.

In organic chemistry, it serves as a precursor for the preparation of complex molecules, especially in asymmetric synthesis, where its chiral nature is exploited to induce stereoselectivity in reactions.

Additionally, i

Used in pharmaceutical research as a chiral building block for the synthesis of active pharmaceutical ingredients (APIs). It is particularly valuable in the development of drugs targeting the central nervous system due to its structural similarity to certain neurotransmitters.

In organic chemistry, it serves as a precursor for the preparation of complex molecules, especially in asymmetric synthesis, where its chiral nature is exploited to induce stereoselectivity in reactions.

Additionally, it is employed in the study of enzyme mechanisms and receptor binding, aiding in the design of more effective and selective therapeutic agents. Its thiophene moiety makes it a useful intermediate in the development of compounds with potential anti-inflammatory or antimicrobial properties.

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