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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

N-[(3R,5S,6R)-2-[(2R,3S,4S,5R,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(3R,5R)-1,2,5-trihydroxy-6-oxo-4-[(2S,3S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyhexan-3-yl]oxyoxan-4-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(3R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]acetamide

O=CC(C(C(C(CO)O)OC1OC(CO)C(C(C1O)OC1OC(CO)C(C(C1NC(=O)C)OC1OC(CO)C(C(C1O)O)O)O)O)OC1OC(C)C(C(C1O)O)O)O Request for Quotation
Chemical Name: N-[(3R,5S,6R)-2-[(2R,3S,4S,5R,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(3R,5R)-1,2,5-trihydroxy-6-oxo-4-[(2S,3S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyhexan-3-yl]oxyoxan-4-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(3R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]acetamide
CAS Number: 60254-64-0
Product Number: AG00EC0K(AGN-PC-09TKDP)
Synonyms:
MDL No:
Molecular Formula: C32H55NO25
Molecular Weight: 853.7708

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Chemical Structure


Lacto-N-fucopentaose V, a type of fucosylated oligosaccharide, plays a crucial role in chemical synthesis as a versatile building block. This unique molecule possesses a specific arrangement of fucose and N-acetylglucosamine residues, making it a valuable tool for designing and creating complex carbohydrate structures.In chemical synthesis, Lacto-N-fucopentaose V can be utilized as a key component in the construction of bioactive compounds, glycoconjugates, and pharmaceutical intermediates. Its precise structure allows for targeted modification and fine-tuning of desired properties, such as enhancing biological activity, improving solubility, and increasing stability.By incorporating Lacto-N-fucopentaose V into synthetic strategies, chemists can access a wide range of diversified carbohydrates and glycoconjugates with tailor-made functionalities. This advanced glycan structure serves as a strategic scaffold for creating novel molecules with potential applications in drug discovery, glycobiology, and biotechnology.