1072108-34-9|O-beta-D-Mannopyranosyl-(1→3)-O-[beta-D-mannopyranosyl-(1→6)]-O-beta-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-D-glucose

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O-beta-D-Mannopyranosyl-(1→3)-O-[beta-D-mannopyranosyl-(1→6)]-O-beta-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-D-glucose | CAS:1072108-34-9

O-beta-D-Mannopyranosyl-(1→3)-O-[beta-D-mannopyranosyl-(1→6)]-O-beta-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-D-glucose

Name：O-beta-D-Mannopyranosyl-(1→3)-O-[beta-D-mannopyranosyl-(1→6)]-O-beta-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1→4)-2-(acetylamino)-2-deoxy-D-glucose
CAS：1072108-34-9
Synonyms：
Molecular Formula：C₃₄H₅₈N₂O₂₆
Molecular Weight：910.82
EINESC：

Description

Properties

Density	1.70±0.1 g/cm3 (20 ºC

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Source	SDS/MSDS Samples
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Synthetic Route

Name	CAS

Articles

Peer-Reviewed Papers

An Expedient Route to the Quinolone Antibacterial Intermediate, 2, 4, 5-Trifluorobenzoic Acid. O'Reilly NJ, et al. Synlett, 1990(10), 609-610 (1990) Synthesis and structure-activity relationships of 4-amino-5-chloro-N-(1,4-dialkylhexahydro-1,4-diazepin-6-yl)-2-methoxybenzamide derivatives, novel and potent serotonin 5-HT3 and dopamine D2 receptors dual antagonist.Yoshimi Hirokawa et al.Chemical & pharmaceutical bulletin, 50(7), 941-959 (2002-07-20)

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Name	CAS

Description

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SDS

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