CAS 66967-01-9

(3R,4S)-N-boc-4-amino-3-hydroxy-6-methyl heptanoic acid

Description:

(3R,4S)-N-boc-4-amino-3-hydroxy-6-methyl heptanoic acid is a chiral amino acid derivative characterized by its specific stereochemistry and functional groups. The "N-boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group, which is commonly used in peptide synthesis to protect amines. The compound features a hydroxyl group (-OH) at the 3-position and an amino group (-NH2) at the 4-position of the heptanoic acid backbone, contributing to its hydrophilic properties. The presence of a methyl group at the 6-position adds to its structural complexity and can influence its biological activity. This compound is typically utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules, due to its ability to serve as a building block for more complex structures. Its specific stereochemistry is crucial for its interaction with biological systems, making it a valuable compound in medicinal chemistry and drug design.

Formula: C₁₃H₂₅NO₅

Synonyms:

• (3R,4S)-4-(N-tert-butoxycarbonyl)amino-3-hydroxy-6-methylheptanoic acid
• Boc-(3R,4S)Sta-OH
• Boc-Sta(3R,4S)-OH
• Boc-Epi-Statine

Boc-Sta(3R,4S)-OH

CAS: 66967-01-9

Ref: 7W-GM8237

(3R,4S)-3-HYDROXY-6-METHYL-4-[(2-METHYLPROPAN-2-YL)OXYCARBONYLAMINO]HEPTANOIC ACID

CAS: 66967-01-9

Purity: 97.0%

Molecular weight: 275.3450012207031

Ref: 10-F513993

Boc-epi-statine (3R,4S)-4-(Boc-amino)-3-hydroxy-6-methyl-heptanoic acid

CAS: 66967-01-9

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Formula: C₁₃H₂₅NO₅

Purity: Min. 95%

Molecular weight: 275.34 g/mol

Ref: 3D-FB107926