The chemical substance known as (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-hept-6-enoic acid, with the CAS number 288617-73-2, is an amino acid derivative characterized by the presence of a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound features a heptenoic acid backbone, which includes a double bond, contributing to its reactivity and potential applications in organic synthesis and peptide chemistry. The Fmoc group is commonly used in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The stereochemistry at the 2-position, indicated by the (2S) designation, suggests that this compound has specific spatial arrangements that may influence its biological activity and interactions. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis, where it can serve as a building block for more complex molecules. Its unique structure and functional groups make it a valuable tool for researchers in developing new therapeutic agents.

(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-hept-6-enoic acid

288617-73-2: (S)-N-Fmoc-α-(4-pentenyl)alanine, 288617-73-2, L B656 Hhj H1Ovmx1&Vq4U1, N-Fmoc-α-(4-Pentenyl)-L-alanine, (S)-N-(9-Fluorenylmethylcarbamate)-2-(2'-pentenyl)alanine, (S)-2-(9H-Fluoren-9-Ylmethoxycarbonylamino)-2-Methyl-Hept-6-Enoic Acid, (S)-2-(((9H-Fluoren-9-Yl)Methoxy)Carbonylamino)-2-Methylhept-6-Enoic Acid

CAS 288617-73-2: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-hept-6-enoic acid

6-Heptenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-, (2S)-

Ref: IN-DA002WVC

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylhept-6-enoic acid

Ref: 10-F213744

Fmoc-(S)-2-(4-pentenyl)alanine

Ref: 54-BICR150