(1S,2R)-2-Aminocyclohexanecarboxylic acid hydrochloride

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Reagent Code: #36241
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CAS Number 158414-45-0

science Other reagents with same CAS 158414-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.6446 g/mol
Formula C₇H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD04112720
thermostat Physical Properties
Melting Point 233 °C
Boiling Point 280 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.133g/cm3
Storage room temperature

description Product Description

(1S,2R)-2-Aminocyclohexanecarboxylic acid hydrochloride is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the development of various biologically active compounds, including peptides and small molecule drugs. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure substances, which are crucial for creating drugs with specific therapeutic effects. Additionally, it is utilized in the study of enzyme mechanisms and receptor interactions due to its structural similarity to natural amino acids. This compound is also explored in the development of novel antibiotics and antiviral agents, leveraging its unique chemical properties to enhance drug efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,032.00

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(1S,2R)-2-Aminocyclohexanecarboxylic acid hydrochloride
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(1S,2R)-2-Aminocyclohexanecarboxylic acid hydrochloride is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the development of various biologically active compounds, including peptides and small molecule drugs. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure substances, which are crucial for creating drugs with specific therapeutic effects. Additionally, it is utilized in the study of enzyme mechanisms a

(1S,2R)-2-Aminocyclohexanecarboxylic acid hydrochloride is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the development of various biologically active compounds, including peptides and small molecule drugs. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure substances, which are crucial for creating drugs with specific therapeutic effects. Additionally, it is utilized in the study of enzyme mechanisms and receptor interactions due to its structural similarity to natural amino acids. This compound is also explored in the development of novel antibiotics and antiviral agents, leveraging its unique chemical properties to enhance drug efficacy and selectivity.

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