CAS 2296988-69-5
:Fmoc-3,3-difluorocyclobutane-1-carboxylic acid
Description:
Fmoc-3,3-difluorocyclobutane-1-carboxylic acid is a chemical compound characterized by its unique structure, which includes a cyclobutane ring substituted with two fluorine atoms and a carboxylic acid functional group. The presence of the Fmoc (9-fluorenylmethoxycarbonyl) group indicates its use in peptide synthesis, particularly as a protective group for amino acids. This compound is notable for its fluorinated cyclobutane moiety, which can impart distinct electronic and steric properties, potentially influencing reactivity and solubility. The difluorination enhances its lipophilicity and may affect its biological activity. As a carboxylic acid, it can participate in various chemical reactions, including esterification and amidation. The compound's CAS number, 2296988-69-5, allows for precise identification in chemical databases. Overall, Fmoc-3,3-difluorocyclobutane-1-carboxylic acid is of interest in synthetic organic chemistry and medicinal chemistry due to its structural features and potential applications in drug development and peptide synthesis.
Formula:C21H19F2NO4
Synonyms:- Cyclobutanecarboxylic acid, 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]methylamino]-3,3-difluoro-
- Fmoc-3,3-difluorocyclobutane-1-carboxylic acid
- 1-({[(9H-fluoren-9-yl)methoxy]carbonyl}(methyl)amino)-3,3-difluorocyclobutane-1-carboxylic acid
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Found 2 products.
1-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-difluorocyclobutane-1-carboxylic acid
CAS:1-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-difluorocyclobutane-1-carboxylic acidFormula:C21H19F2NO4Purity:98%Molecular weight:387.381-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-difluorocyclobutane-1-carboxylic acid
CAS:Purity:98%Molecular weight:387.13
