1-Amino-3-methylcyclohexane-1-carboxylic acid

≥95%

Reagent Code: #132290
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CAS Number 55550-84-0

science Other reagents with same CAS 55550-84-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.21 g/mol
Formula C₈H₁₅NO₂
badge Registry Numbers
MDL Number MFCD01745645
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its rigid cyclohexane backbone with functional groups in defined stereochemistry makes it valuable in designing drugs targeting neurological and metabolic disorders. It is also employed in the preparation of peptidomimetics, where it helps enhance metabolic stability and receptor selectivity. Additionally, it serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational restraint and hydrogen-bonding capabilities.

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inventory 1g
10-20 days ฿42,170.00

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1-Amino-3-methylcyclohexane-1-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its rigid cyclohexane backbone with functional groups in defined stereochemistry makes it valuable in designing drugs targeting neurological and metabolic disorders. It is also employed in the preparation of peptidomimetics, where it helps enhance metabolic stability and receptor selectivity. Additionally, it serves as a building block in medicinal chemistry for st

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its rigid cyclohexane backbone with functional groups in defined stereochemistry makes it valuable in designing drugs targeting neurological and metabolic disorders. It is also employed in the preparation of peptidomimetics, where it helps enhance metabolic stability and receptor selectivity. Additionally, it serves as a building block in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational restraint and hydrogen-bonding capabilities.

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