MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL])

  • CasNo:71496-53-2
  • purity:99%
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Manufacturer supply MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) 71496-53-2 with sufficient stock and high standard We supply high quality MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) (CAS 71496-53-2), in stock, factory directly supply to clients, lower prices, more competitiveness.

What is the MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) ?

MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) is , while it's Molecular Formula is C62H104 N4 O46. is used in preparation of Heterocyclic Boronic Acid derivatives or their conjugates with functional molecules as mono- or multivalent ligands with specific binding selectivity to Sialic Acids.

What is the CAS number for MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) ?

The CAS number of MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) is 71496-53-2.

More information of MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) 71496-53-2 are:

Synonyms

[GAL-GLCNAC]2MAN3[GLCNAC]2;MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]);MANNOTRIOSE-DI-(N-ACETYL-D-*GLUCOSAMINE) , BIS(GALAC;(Gal-GlcNAc)2Man3(GlcNAc)2, Mannotriose-di-(N-acetyl-D-glucosamine), bis(galactosyl-[N-acetyl-D-glucosaminyl])

CAS?Number

71496-53-2

Molecular Formula

C62H104 N4 O46

Molecular Weight

1641.49

PSA

786.90000

LogP

-18.64640

What is MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) (71496-53-2) used for?

MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL]) is a complex carbohydrate structure composed of a trisaccharide core with two N-acetyl-D-glucosamine units and two bis(galactosyl-N-acetyl-D-glucosaminyl) branches. It is known for its specific binding selectivity to Sialic Acids, making it a valuable compound in the development of heterocyclic boronic acid derivatives and their conjugates.

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