CAS 101669-78-7

4-(N-Boc-amino)-3-oxo-pentanoic Acid Methyl Ester

Description:

4-(N-Boc-amino)-3-oxo-pentanoic Acid Methyl Ester, with the CAS number 101669-78-7, is a chemical compound characterized by its functional groups and structural features. It contains a Boc (tert-butyloxycarbonyl) protecting group on the amino functionality, which is commonly used in peptide synthesis to protect amines. The presence of a keto group (3-oxo) indicates that it has a carbonyl functionality, contributing to its reactivity and potential applications in organic synthesis. The methyl ester group suggests that it can undergo hydrolysis to yield the corresponding carboxylic acid, making it versatile for further chemical transformations. This compound is typically utilized in the synthesis of peptides and other bioactive molecules due to its ability to facilitate coupling reactions. Its solubility in organic solvents and stability under various conditions make it a valuable intermediate in medicinal chemistry and drug development. Overall, its unique structure and functional groups provide a foundation for diverse chemical applications.

Formula: C₁₁H₁₉NO₅

Synonyms:

• Methyl 4-N-(tert-Butoxycarbonyl)amino-3-oxopentanoat
• Methyl 4-N-(tert-Butoxycarbonyl)amino-3-oxopentanoate

Pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, methyl ester, (4S)-

CAS: 101669-78-7

Formula: C₁₁H₁₉NO₅

Color and Shape: Solid

Molecular weight: 245.2723

Ref: IN-DA00054Y

4-(N-Boc-amino)-3-oxo-pentanoic acid methyl ester

CAS: 101669-78-7

Molecular weight: 245.27

Ref: 7W-GM5384

4-(N-Boc-amino)-3-oxo-pentanoic Acid Methyl Ester

Controlled Product

CAS: 101669-78-7

Applications 4-(N-Boc-amino)-3-oxo-pentanoic Acid Methyl Ester (cas# 101669-78-7) is a compound useful in organic synthesis.
References Birch, O.M., et al.: J. Biol. Chem., 270, 19 (1995),

Formula: C₁₁H₁₉NO₅

Color and Shape: Neat

Molecular weight: 245.27

Ref: TR-B620980