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CAS 1003599-68-5: Bis(phenylmethyl) P-[3-[acetyl(phenylmethoxy)amino]propyl]phosphonate
Formula:C26H30NO5P
InChI:InChI=1S/C26H30NO5P/c1-23(28)27(30-20-24-12-5-2-6-13-24)18-11-19-33(29,31-21-25-14-7-3-8-15-25)32-22-26-16-9-4-10-17-26/h2-10,12-17H,11,18-22H2,1H3
InChI key:InChIKey=XRFOPUVTELUIOT-UHFFFAOYSA-N
SMILES:P(OCC1=CC=CC=C1)(OCC2=CC=CC=C2)(CCCN(OCC3=CC=CC=C3)C(C)=O)=O
Synonyms:- Bis(phenylmethyl) P-[3-[acetyl(phenylmethoxy)amino]propyl]phosphonate
- Phosphonic acid, P-[3-[acetyl(phenylmethoxy)amino]propyl]-, bis(phenylmethyl) ester
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Tri-O-benzyl FR 900098
CAS:Tri-O-benzyl FR 900098 is a chemical compound, often referenced in biochemical research contexts. It is a synthetic derivative that originates from complex chemical synthesis, involving multiple benzylation steps to modify the original molecular framework. This structural transformation lends the compound unique chemical properties. The mode of action of Tri-O-benzyl FR 900098 involves interactions at a molecular level, often serving as a substrate or an inhibitor in enzymatic studies. Its distinctive benzylated structure allows it to fit into active sites of enzymes with high specificity, enabling researchers to study enzyme activity, inhibition, and protein-ligand interactions. In terms of applications, Tri-O-benzyl FR 900098 is utilized extensively in the field of enzymology and structural biology. Its properties make it an ideal candidate for probing enzyme mechanisms, testing hypotheses related to enzyme specificity, and studying the impacts of structural modifications on activity. This compound thus plays a crucial role in advancing our understanding of biochemical pathways and the development of novel therapeutics.Formula:C26H30NO5PPurity:Min. 95%Molecular weight:467.49 g/mol