CAS 218457-73-9: Hexanedioic acid,2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2R)- (9CI)

Description: Hexanedioic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2R)- (9CI), commonly referred to as a derivative of hexanedioic acid, features a hexanedioic acid backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group attached to an amino group. This compound is characterized by its dual functionality, possessing both carboxylic acid and amine groups, which allows it to participate in various chemical reactions, including peptide synthesis. The Fmoc group is widely used in solid-phase peptide synthesis due to its stability under basic conditions and ease of removal under acidic conditions. The (2R) designation indicates the specific stereochemistry at the chiral center, which can influence the compound's reactivity and interaction with biological systems. This compound is typically utilized in organic synthesis and biochemistry, particularly in the development of peptide-based therapeutics and research applications. Its unique structure and functional groups make it a valuable intermediate in the synthesis of more complex molecules.

Formula: C₂₁H₂₁NO₆

Synonyms:

• Fmoc-D-2-Aminoadipic Acid
• Fmoc-D-Homoglutamic Acid
• Fmoc-D-Aad-Oh
• Fmoc-D-Alpha-Aminoadipic Acid
• N-Alpha-(9-Fluorenylmethoxycarbonyl)-Alpha-D-Aminoadipic Acid
• Fmoc-(R)-2-aminoadipic acid

Fmoc-D-a-aminoadipic acid

CAS: 218457-73-9

• Purity: 98.0%
• Molecular weight: 383.3999938964844

Fmoc-D-a-aminoadipic acid

CAS: 218457-73-9

Please enquire for more information about Fmoc-D-a-aminoadipic acid including the price, delivery time and more …

• Formula: C₂₁H₂₁NO₆
• Purity: Min. 95%
• Molecular weight: 383.39 g/mol