Carbamic acid, specifically the compound with the name "[(1S)-2-[[(1S)-3-diazo-1-methyl-2-oxopropyl]amino]-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-,9H-fluoren-9-ylmethyl ester (9CI)" and CAS number 205763-22-0, is a complex organic molecule characterized by its carbamate functional group. This compound features a diazo group, which is notable for its reactivity and potential applications in organic synthesis. The presence of a fluorenylmethyl ester indicates that it may exhibit unique properties related to its aromatic structure, potentially influencing its solubility and stability. Additionally, the molecule contains multiple functional groups, including an amino group and a hydroxyl group, which can participate in various chemical reactions, making it versatile in synthetic chemistry. Its stereochemistry, indicated by the (1S) configuration, suggests specific spatial arrangements that may affect its biological activity and interactions. Overall, this compound's intricate structure and functional diversity position it as a candidate for research in medicinal chemistry and related fields.

Carbamic acid,[(1S)-2-[[(1S)-3-diazo-1-methyl-2-oxopropyl]amino]-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-,9H-fluoren-9-ylmethyl ester (9CI)

205763-22-0: Carbamic acid, specifically the compound with the name "[(1S)-2-[[(1S)-3-diazo-1-methyl-2-oxopropyl]amino]-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-,9H-fluoren-9-ylmethyl ester (9CI)" and CAS number 205763-22-0, is a complex organic molecule characterized by its carbamate functional group. This compound features a diazo group, which is notable for its reactivity and potential applications in organic synthesis. The presence of a fluorenylmethyl ester indicates that it may exhibit unique properties related to its aromatic structure, potentially influencing its solubility and stability. Additionally, the molecule contains multiple functional groups, including an amino group and a hydroxyl group, which can participate in various chemical reactions, making it versatile in synthetic chemistry. Its stereochemistry, indicated by the (1S) configuration, suggests specific spatial arrangements that may affect its biological activity and interactions. Overall, this compound's intricate structure and functional diversity position it as a candidate for research in medicinal chemistry and related fields.

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CAS 205763-22-0

Carbamic acid,[(1S)-2-[[(1S)-3-diazo-1-methyl-2-oxopropyl]amino]-1-[(4-hydroxyphenyl)methyl]-2-oxoethyl]-,9H-fluoren-9-ylmethyl ester (9CI)

Fmoc-Tyr-Ala-diazomethylketone

Ref: 3D-FF111337