Boc-D-Dab(Fmoc)-OH, with the CAS number 131570-57-5, is a protected amino acid derivative commonly used in peptide synthesis. It features a Boc (tert-butyloxycarbonyl) protecting group on the amino group and an Fmoc (9-fluorenylmethoxycarbonyl) protecting group on the side chain of the amino acid. This compound is characterized by its stability under basic conditions, making it suitable for various synthetic applications. The presence of both Boc and Fmoc groups allows for selective deprotection steps, facilitating the synthesis of complex peptides. The D-Dab (D-2,4-diaminobutyric acid) structure contributes to its unique properties, including the ability to introduce cationic charges into peptides, which can enhance solubility and biological activity. Additionally, Boc-D-Dab(Fmoc)-OH is typically white to off-white in appearance and is soluble in organic solvents like dimethylformamide (DMF) and dimethyl sulfoxide (DMSO). Its applications extend to drug development and the study of peptide interactions in biological systems.

Boc-D-Dab(Fmoc)-OH

131570-57-5: (2R)-2-(tert-butoxycarbonylamino)-4-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid

Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2R)-

(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoic acid

Please enquire for more information about N-alpha-Boc-Ngamma-Fmoc-D-2,4-diaminobutyric acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

CAS 131570-57-5: Boc-D-Dab(Fmoc)-OH

Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2R)-

Ref: IN-DA000ZG0

(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoic acid

Ref: 54-OR74663

Boc-D-Dab(Fmoc)-OH

Ref: 10-F019575

N-α-Boc-Nγ-Fmoc-D-2,4-diaminobutyric acid

Ref: 3D-FB48826

Boc-D-Dab(Fmoc)-OH

Ref: 01-4027507