The chemical substance known as (2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propanoate, with the CAS number 200395-72-8, is a complex organic compound characterized by its unique structural features. It contains a pentafluorophenyl group, which contributes to its high electronegativity and potential for strong interactions with other molecules. The presence of a fluorenylmethoxycarbonyl (Fmoc) group indicates its application in peptide synthesis, particularly as a protective group for amino acids. The tritylsulfanyl moiety suggests that it may have applications in organic synthesis or as a protecting group in various chemical reactions. This compound is likely to exhibit significant hydrophobic characteristics due to the presence of multiple aromatic rings and fluorinated groups, which can influence its solubility and reactivity. Additionally, the stereochemistry indicated by the (2S) configuration suggests specific spatial arrangements that may affect its biological activity and interactions with other chemical entities. Overall, this compound is of interest in synthetic organic chemistry and potentially in pharmaceutical applications.

(2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propanoate

200395-72-8: The chemical substance known as (2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propanoate, with the CAS number 200395-72-8, is a complex organic compound characterized by its unique structural features. It contains a pentafluorophenyl group, which contributes to its high electronegativity and potential for strong interactions with other molecules. The presence of a fluorenylmethoxycarbonyl (Fmoc) group indicates its application in peptide synthesis, particularly as a protective group for amino acids. The tritylsulfanyl moiety suggests that it may have applications in organic synthesis or as a protecting group in various chemical reactions. This compound is likely to exhibit significant hydrophobic characteristics due to the presence of multiple aromatic rings and fluorinated groups, which can influence its solubility and reactivity. Additionally, the stereochemistry indicated by the (2S) configuration suggests specific spatial arrangements that may affect its biological activity and interactions with other chemical entities. Overall, this compound is of interest in synthetic organic chemistry and potentially in pharmaceutical applications.

CAS 200395-72-8

(2,3,4,5,6-pentafluorophenyl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propanoate

Fmoc-D-Cys(Trt)-OPfp

Ref: 01-4017508

Fmoc-D-Cys(Trt)-OPfp

Ref: IN-DA002CQJ

Fmoc-S-trityl-D-cysteine pentafluorophenyl ester

Ref: 7W-GM6691