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CAS 13089-19-5

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α-D-Glucopyranoside, phenyl 2-(acetylamino)-2-deoxy-, 3,4,6-triacetate

Description:
α-D-Glucopyranoside, phenyl 2-(acetylamino)-2-deoxy-, 3,4,6-triacetate, commonly referred to as a derivative of glucosamine, is a carbohydrate compound characterized by its glucopyranoside structure, which features a six-membered ring of carbon atoms with hydroxyl groups. This specific compound includes an acetylamino group, indicating the presence of an acetylated amine, which contributes to its biological activity and solubility properties. The triacetate designation signifies that three hydroxyl groups on the glucopyranose ring are acetylated, enhancing its lipophilicity and stability. This compound is typically used in biochemical research and synthesis, particularly in the study of glycosylation reactions and carbohydrate chemistry. Its molecular structure allows for interactions with various biological molecules, making it relevant in pharmacological applications. The CAS number 13089-19-5 uniquely identifies this compound, facilitating its recognition in chemical databases and literature. Overall, this substance exemplifies the complexity and versatility of carbohydrate derivatives in scientific research.
Formula:C20H25NO9
InChI:InChI=1S/C20H25NO9/c1-11(22)21-17-19(28-14(4)25)18(27-13(3)24)16(10-26-12(2)23)30-20(17)29-15-8-6-5-7-9-15/h5-9,16-20H,10H2,1-4H3,(H,21,22)/t16-,17-,18-,19-,20+/m1/s1
InChI key:InChIKey=RTIVQWVVADQPHA-WAPOTWQKSA-N
SMILES:O(C(C)=O)[C@@H]1[C@@H](NC(C)=O)[C@@H](OC2=CC=CC=C2)O[C@H](COC(C)=O)[C@H]1OC(C)=O
Synonyms:
  • Glucopyranoside, phenyl 2-acetamido-2-deoxy-, triacetate
  • Phenyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranoside
  • α-D-Glucopyranoside, phenyl 2-(acetylamino)-2-deoxy-, 3,4,6-triacetate
  • Glucopyranoside, phenyl 2-acetamido-2-deoxy-, triacetate (ester), α-D-
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