(S)-Methyl 3-amino-3-(2-methoxyphenyl)propanoate hydrochloride

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Reagent Code: #38435
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CAS Number 1391398-83-6

science Other reagents with same CAS 1391398-83-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.70 g/mol
Formula C₁₁H₁₆ClNO₃
badge Registry Numbers
MDL Number MFCD12911028
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring an amino group and a methoxyphenyl moiety, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs) that target neurological and psychiatric disorders. It is often employed in the creation of compounds that interact with neurotransmitter systems, such as serotonin and dopamine receptors, due to its potential to modulate these pathways. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing efficacy and reducing side effects in therapeutic applications. Researchers also explore its use in asymmetric synthesis, where it serves as a building block for complex organic molecules with high stereochemical precision.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,368.00
inventory 250mg
10-20 days ฿20,745.00

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(S)-Methyl 3-amino-3-(2-methoxyphenyl)propanoate hydrochloride
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring an amino group and a methoxyphenyl moiety, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs) that target neurological and psychiatric disorders. It is often employed in the creation of compounds that interact with neurotransmitter systems, such as serotonin and dopamine receptors, due to its potential to mo

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring an amino group and a methoxyphenyl moiety, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs) that target neurological and psychiatric disorders. It is often employed in the creation of compounds that interact with neurotransmitter systems, such as serotonin and dopamine receptors, due to its potential to modulate these pathways. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, enhancing efficacy and reducing side effects in therapeutic applications. Researchers also explore its use in asymmetric synthesis, where it serves as a building block for complex organic molecules with high stereochemical precision.

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