Boc-Asp(OFm)-OH, with the CAS number 117014-32-1, is a derivative of aspartic acid, an amino acid that plays a crucial role in various biological processes. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in peptide synthesis, which helps to prevent unwanted reactions during the synthesis process. The "OFm" indicates the presence of a methoxy group attached to the phenyl ring, which can influence the compound's solubility and reactivity. This compound is typically utilized in the field of organic chemistry and peptide synthesis, particularly in the preparation of peptides where selective protection of functional groups is necessary. Its characteristics include being a white to off-white solid, soluble in organic solvents, and relatively stable under standard laboratory conditions. The presence of the Boc group allows for easy deprotection under acidic conditions, facilitating further chemical transformations. Overall, Boc-Asp(OFm)-OH serves as an important intermediate in the synthesis of more complex biomolecules.

Boc-Asp(OFm)-OH

117014-32-1: N-alpha-tert-Butyloxycarbonyl-aspartic acid gamma-fluorenylmethyl ester, BA-gamma-Fme, Nalpha-Boc-asp-gamma-fluorenylmethyl ester, L-Aspartic acid, N-((1,1-dimethylethoxy)carbonyl)-, 4-(9H-fluoren-9-ylmethyl) ester, (2S)-2-[(tert-butoxycarbonyl)amino]-4-(9H-fluoren-9-ylmethoxy)-4-oxobutanoic acid (non-preferred name)

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CAS 117014-32-1: Boc-Asp(OFm)-OH

Boc-Asp(OFm)-OH

Ref: 01-4015227

Boc-L-aspartic acid β-9-fluorenylmethyl ester

Ref: 3D-FB47477

(2S)-2-[(tert-butoxycarbonyl)amino]-4-(9H-fluoren-9-ylmethoxy)-4-oxobutanoic acid

Ref: 10-F609184

L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(9H-fluoren-9-ylmethyl) ester

Ref: IN-DA000DJM

(2S)-2-[(tert-butoxycarbonyl)amino]-4-(9H-fluoren-9-ylmethoxy)-4-oxobutanoic acid

Ref: 54-OR95547