CAS 214206-61-8: 2-(tert-Butoxycarbonylamino)hex-5-enoic acid

Description: 2-(tert-Butoxycarbonylamino)hex-5-enoic acid is an organic compound characterized by its unique structure, which includes a hexenoic acid backbone with a tert-butoxycarbonyl (Boc) protecting group attached to an amino group. This compound features a double bond in the hexene chain, contributing to its reactivity and potential applications in organic synthesis. The Boc group serves as a protective moiety for the amino functionality, allowing for selective reactions without interfering with the amine. The presence of the carboxylic acid group imparts acidic properties, making it soluble in polar solvents and reactive in various chemical transformations. This compound is often utilized in peptide synthesis and other organic reactions where protection of the amine is necessary. Its specific stereochemistry and functional groups can influence its behavior in biological systems, making it of interest in medicinal chemistry and drug development. Overall, 2-(tert-Butoxycarbonylamino)hex-5-enoic acid is a versatile intermediate in synthetic organic chemistry.

Formula: C₁₁H₁₉NO₄

InChI: InChI=1/C11H19NO4/c1-5-6-7-8(9(13)14)12-10(15)16-11(2,3)4/h5,8H,1,6-7H2,2-4H3,(H,12,15)(H,13,14)

Synonyms:

• 5-Hexenoic Acid, 2-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-

2-((tert-Butoxycarbonyl)amino)hex-5-enoic acid

CAS: 214206-61-8

• Formula: C₁₁H₁₉NO₄
• Purity: 97%
• Molecular weight: 229.2729

2-((Tert-butoxycarbonyl)amino)hex-5-enoic acid

CAS: 214206-61-8

• Purity: 98%
• Molecular weight: 229.2760009765625

2-(tert-Butoxycarbonylamino)hex-5-enoic acid

CAS: 214206-61-8

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• Formula: C₁₁H₁₉NO₄
• Purity: Min. 95%
• Molecular weight: 229.27 g/mol