CAS 126587-35-7

(S)-4-[[(tert-Butoxy)carbonyl]amino]-5-hydroxypentanoic acid methyl ester

Description:

(S)-4-[[(tert-Butoxy)carbonyl]amino]-5-hydroxypentanoic acid methyl ester, with CAS number 126587-35-7, is a chiral amino acid derivative characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group on the amino group and a methyl ester functional group at the carboxylic acid end. This compound features a five-carbon backbone with a hydroxyl group at the fifth position, contributing to its hydrophilicity and potential for forming hydrogen bonds. The presence of the Boc group enhances its stability and solubility in organic solvents, making it useful in peptide synthesis and other organic reactions. The chirality of the molecule indicates that it exists in two enantiomeric forms, with the (S) configuration being biologically relevant in many contexts, particularly in pharmaceuticals. Its structural features suggest potential applications in drug development, particularly in the design of bioactive compounds that require specific stereochemistry for optimal activity. Overall, this compound exemplifies the complexity and utility of amino acid derivatives in synthetic organic chemistry.

Formula: C₁₁H₂₁NO₅

InChI: InChI=1/C11H21NO5/c1-11(2,3)17-10(15)12-8(7-13)5-6-9(14)16-4/h8,13H,5-7H2,1-4H3,(H,12,15)/t8-/m0/s1

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

Synonyms:

• Methyl (4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentanoate
• pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-hydroxy-, methyl ester, (4S)-

(S)-Methyl 4-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate

CAS: 126587-35-7

Formula: C₁₁H₂₁NO₅

Purity: 95%

Color and Shape: Solid

Molecular weight: 247.2881

Ref: IN-DA000SYM

Methyl (S)-4-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate

CAS: 126587-35-7

Purity: >95%

Molecular weight: 247.2910004

Ref: 10-F725458