MANNOTRIOSE-DI-(N-ACETYL-D-GLUCOSAMINE), BIS(GALACTOSYL-[N-ACETYL-D-GLUCOSAMINYL])
- CasNo:71496-53-2
- purity:99%
Details
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:
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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]) |
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CAS?Number |
71496-53-2 |
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Molecular Formula |
C62H104 N4 O46 |
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Molecular Weight |
1641.49 |
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PSA |
786.90000 |
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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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