CAS 94888-34-3

Boc-L-isoleucine amide

Description:

Boc-L-isoleucine amide is a derivative of isoleucine, an essential amino acid, characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group and an amide functional group. This compound is typically utilized in peptide synthesis and as an intermediate in the preparation of various bioactive molecules. The Boc group serves to protect the amino functionality during synthetic procedures, allowing for selective reactions at other functional sites. Boc-L-isoleucine amide is generally a white to off-white solid, and its solubility can vary depending on the solvent used, often being soluble in polar organic solvents. The compound is stable under standard laboratory conditions but may require careful handling to avoid hydrolysis of the amide bond. Its molecular structure contributes to its role in influencing the conformation and biological activity of peptides, making it significant in medicinal chemistry and biochemistry.

Formula: C₁₁H₂₂N₂O₃

InChI: InChI=1/C11H22N2O3/c1-6-7(2)8(9(12)14)13-10(15)16-11(3,4)5/h7-8H,6H2,1-5H3,(H2,12,14)(H,13,15)/t7?,8-/m0/s1

SMILES: CCC(C)[C@@H](C(=N)O)N=C(O)OC(C)(C)C

Synonyms:

• Boc-L-Ile-NH2
• N-tert-Butoxycarbonyl-L-isoleucine amide

N-tert-Butoxycarbonyl-L-isoleucineamide

CAS: 94888-34-3

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Formula: C₁₁H₂₂N₂O₃

Purity: Min. 95%

Color and Shape: Solid

Molecular weight: 230.3 g/mol

Ref: 3D-FB151479