CAS 270596-34-4

(βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-furanbutanoic acid

Description:

(βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-furanbutanoic acid, commonly referred to as Fmoc-2-furanbutanoic acid, is a chemical compound characterized by its unique structure that includes a furan ring and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is primarily utilized in peptide synthesis as a building block, where the Fmoc group serves as a protective moiety for the amino group, allowing for selective reactions during the synthesis process. The presence of the furan moiety contributes to its reactivity and potential applications in organic synthesis. The compound is typically a solid at room temperature and is soluble in organic solvents, making it suitable for various laboratory applications. Its chirality, indicated by the (βR) designation, suggests that it exists in a specific stereoisomeric form, which can influence its biological activity and interactions. Overall, this compound is significant in the field of medicinal chemistry and peptide research due to its functional groups and structural properties.

Formula: C₂₃H₂₁NO₅

InChI: InChI=1S/C23H21NO5/c25-22(26)13-15(12-16-6-5-11-28-16)24-23(27)29-14-21-19-9-3-1-7-17(19)18-8-2-4-10-20(18)21/h1-11,15,21H,12-14H2,(H,24,27)(H,25,26)/t15-/m1/s1

InChI key: InChIKey=YIYJEKXVMOCXPC-OAHLLOKOSA-N

SMILES: C(OC(N[C@H](CC1=CC=CO1)CC(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3

Synonyms:

• (3R)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-furan-2-ylbutanoic acid
• (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(furan-2-yl)butyric acid
• (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-furanbutanoic acid
• 2-Furanbutanoic acid, β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βR)-

Fmoc-(r)-3-amino-4-(2-furyl)-butyric acid

CAS: 270596-34-4

Formula: C₂₃H₂₁NO₅

Purity: 95%

Molecular weight: 391.4165

Ref: IN-DA00BCWT