The chemical substance known as (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoic acid hydrochloride, with the CAS number 1038924-71-8, is a synthetic compound characterized by its chiral centers, which contribute to its specific stereochemistry. This compound features a biphenyl moiety, which enhances its hydrophobic properties, and an amino acid structure that includes both an amino group and a carboxylic acid group, making it a potential candidate for biological activity. The hydrochloride form indicates that it is a salt, which typically improves its solubility in water and stability. The presence of the amino group suggests potential interactions with biological receptors, making it of interest in medicinal chemistry. Its stereochemistry may influence its pharmacokinetics and pharmacodynamics, affecting how it interacts with biological systems. Overall, this compound's unique structure and properties position it as a subject of interest in drug development and biochemical research.

(2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoic acid hydrochloride

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Sacubitril Impurity 11 HCl

(2R,4S)-5-([1,1'-Biphenyl]-4-yl)-4-amino-2-methylpentanoic Acid Hydrochloride

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CAS 1038924-71-8: (2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoic acid hydrochloride

Sacubitril Impurity 11 HCl

Ref: 4Z-S-072018

(2R,4S)-5-([1,1'-Biphenyl]-4-yl)-4-amino-2-methylpentanoic Acid Hydrochloride

Ref: TR-B398175

(2R,4S)-5-([1,1'-Biphenyl]-4-yl)-4-amino-2-Methylpentanoic acid hydrochloride

Ref: 3D-FB180605

Sacubitril Impurity 11

Ref: ST-EA-CP-S18003