CAS 282524-78-1

Benzenebutanoic acid, b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-

Description:

Benzenebutanoic acid, b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]- is a chemical compound characterized by its complex structure, which includes a benzenebutanoic acid moiety and a fluorenylmethoxycarbonyl (Fmoc) protecting group. The Fmoc group is commonly used in peptide synthesis to protect amino groups, allowing for selective reactions. This compound typically exhibits properties associated with both aromatic and aliphatic systems, including potential hydrophobic interactions due to the aromatic ring and polar characteristics from the carboxylic acid functional group. It is likely to be soluble in organic solvents while showing limited solubility in water. The presence of the Fmoc group suggests that this compound may be utilized in the synthesis of peptides or other complex organic molecules. Additionally, the compound may exhibit biological activity, although specific biological properties would depend on its application and context. Overall, its unique structure makes it a valuable intermediate in organic synthesis and medicinal chemistry.

Formula: C₂₅H₂₃NO₄

Synonyms:

• N-Fmoc-3-Amino-4-Phenylbutanoic Acid
• 3-(9 H-Fluoren-9-Ylmethoxycarbonylamino)-4-Phenyl-Butyric Acid
• 3-(9 H-Fluoroen-9-Ylmethoxycarbonylamino)-4-Phenyl-Butyric Acid

3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylbutanoic acid

CAS: 282524-78-1

Formula: C₂₅H₂₃NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 401.4544

Ref: IN-DA007L15

3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylbutanoic acid

CAS: 282524-78-1

3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylbutanoic acid

Purity: 95%

Molecular weight: 401.45g/mol

Ref: 54-OR76236

3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylbutanoic acid

CAS: 282524-78-1

Purity: 97%

Molecular weight: 401.4620056

Ref: 10-F690962