CAS 141743-13-7

NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine

Description:

NALPHA-9-Fluorenylmethoxycarbonyl-N-benzylglycine, commonly referred to as Fmoc-N-benzylglycine, is a chemical compound used primarily in peptide synthesis as a protecting group for amino acids. It features a fluorenylmethoxycarbonyl (Fmoc) group, which is a widely utilized protective group due to its stability under basic conditions and ease of removal under mild acidic conditions. The presence of the benzyl group enhances the lipophilicity of the molecule, which can influence its solubility and reactivity in various organic reactions. This compound is typically employed in solid-phase peptide synthesis, where it helps to prevent unwanted reactions during the assembly of peptide chains. Its structure allows for selective deprotection, facilitating the stepwise construction of peptides. Additionally, the compound's characteristics, such as melting point, solubility, and reactivity, are influenced by the specific functional groups present, making it a valuable tool in synthetic organic chemistry and biochemistry.

Formula: C₂₄H₂₁NO₄

Synonyms:

• N-Fmoc-N-benzyl-glycine

Fmoc,bzl-gly-oh

CAS: 141743-13-7

Formula: C₂₄H₂₁NO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 387.4278

Ref: IN-DA001GZA

N-Fmoc-N-benzyl-glycine

CAS: 141743-13-7

N-Fmoc-N-benzyl-glycine

Purity: 97%

Molecular weight: 387.43g/mol

Ref: 54-OR961573

2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(benzyl)amino)acetic acid

CAS: 141743-13-7

Formula: C₂₄H₂₁NO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 387.435

Ref: 10-F236299