trans-2-Aminocyclohexanecarboxylic acid hydrochloride

95%

Reagent Code: #50640
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CAS Number 57266-57-6

science Other reagents with same CAS 57266-57-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.6446 g/mol
Formula C₇H₁₄ClNO₂
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MDL Number MFCD05863557
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. It serves as a precursor for the synthesis of various biologically active compounds, including peptides and peptidomimetics. Its stereochemistry makes it valuable in asymmetric synthesis, aiding in the creation of enantiomerically pure drugs. Additionally, it is employed in research for developing novel therapeutic agents, especially in the fields of neurology and oncology. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous-based reactions and formulations.

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inventory 100mg
10-20 days ฿6,390.00

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trans-2-Aminocyclohexanecarboxylic acid hydrochloride
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Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. It serves as a precursor for the synthesis of various biologically active compounds, including peptides and peptidomimetics. Its stereochemistry makes it valuable in asymmetric synthesis, aiding in the creation of enantiomerically pure drugs. Additionally, it is employed in research for developing novel therapeutic agents, especially in the fields of neurology and oncology. Its hydrochloride form enha

Used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. It serves as a precursor for the synthesis of various biologically active compounds, including peptides and peptidomimetics. Its stereochemistry makes it valuable in asymmetric synthesis, aiding in the creation of enantiomerically pure drugs. Additionally, it is employed in research for developing novel therapeutic agents, especially in the fields of neurology and oncology. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous-based reactions and formulations.

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