BOC-(S)-2-Amino-4-cyclohexylbutanoic acid, with the CAS number 143415-51-4, is a chemical compound characterized by its structure, which includes a butanoic acid backbone with a cyclohexyl group and a BOC (tert-butyloxycarbonyl) protecting group on the amino functionality. This compound is typically used in peptide synthesis and as an intermediate in organic synthesis due to its ability to protect amino groups during chemical reactions. The presence of the cyclohexyl group contributes to its hydrophobic characteristics, influencing its solubility and interaction with biological systems. The BOC group is commonly employed in the protection of amino acids, allowing for selective reactions without interfering with the amino functionality. This compound is often utilized in pharmaceutical research and development, particularly in the design of bioactive molecules. Its stereochemistry, indicated by the (S) designation, suggests that it has specific spatial arrangements that can affect its biological activity and interactions. Overall, BOC-(S)-2-amino-4-cyclohexylbutanoic acid is a valuable compound in synthetic organic chemistry and medicinal chemistry.

BOC-(S)-2-Amino-4-Cyclohexyl butanoic acid

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(S)-2-((tert-Butoxycarbonyl)amino)-4-cyclohexylbutanoic acid

CAS 143415-51-4: BOC-(S)-2-Amino-4-Cyclohexyl butanoic acid

(S)-2-((tert-Butoxycarbonyl)amino)-4-cyclohexylbutanoic acid

Ref: 54-OR91294

Carfilzomib Impurity 57

Ref: ST-EA-CP-C153049

Carfilzomib Impurity 28

Ref: 4Z-C-121031

2-(TERT-BUTOXYCARBONYLAMINO)-1,2,3,4-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC ACID

Ref: IN-DA00A0HQ

(2S)-2-{[(tert-Butoxy)carbonyl]amino}-4-cyclohexylbutanoic acid

Ref: 3D-TFA41551

(S)-2-((tert-Butoxycarbonyl)amino)-4-cyclohexylbutanoic acid

Ref: 10-F498613