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CAS 132063-04-8

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O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-D-GLUCOPYRANOSYLIDENE)AMINO N-PHENYL CARBAMATE

Description:
O-(2-Acetamido-3,4,6-tri-O-acetyl-D-glucopyranosylidene)amino N-phenyl carbamate, with CAS number 132063-04-8, is a complex organic compound characterized by its carbohydrate and amine functional groups. This substance features a glucopyranosylidene moiety, which is a derivative of glucose, modified with acetyl groups that enhance its solubility and stability. The presence of the acetamido group indicates that it has potential biological activity, possibly related to its interactions with enzymes or receptors. The N-phenyl carbamate portion suggests that it may exhibit properties typical of carbamate compounds, such as potential use in medicinal chemistry or as a biochemical probe. Its structural complexity implies that it may participate in various chemical reactions, including hydrolysis and acylation, and it may also exhibit specific stereochemical configurations due to the presence of multiple chiral centers. Overall, this compound's unique structure positions it as a candidate for further research in fields such as pharmacology and biochemistry.
Formula:C21H25N3O10
InChI:InChI=1/C21H25N3O10/c1-11(25)22-17-19(32-14(4)28)18(31-13(3)27)16(10-30-12(2)26)33-20(17)24-34-21(29)23-15-8-6-5-7-9-15/h5-9,16-19H,10H2,1-4H3,(H,22,25)(H,23,29)/b24-20-/t16?,17-,18+,19+/m0/s1
InChI key:InChIKey=WIPJJKKTCDJFST-NCXUSEDFSA-N
SMILES:O(C(C)=O)[C@@H]1[C@@H](NC(C)=O)C(=NOC(NC2=CC=CC=C2)=O)O[C@H](COC(C)=O)[C@H]1OC(C)=O
Synonyms:
  • D-Gluconimidic acid, 2-(acetylamino)-2-deoxy-N-[[(phenylamino)carbonyl]oxy]-, δ-lactone, 3,4,6-triacetate
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