2α-Mannobiose - Misplaced Pages

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2α-Mannobiose
Names

IUPAC name α-D-Mannopyranosyl-(1→2)-D-mannopyranose
Systematic IUPAC name (2Ξ,3S,4S,5S,6R)-6-(Hydroxymethyl)-2-{oxy}oxane-2,4,5-triol
Identifiers
CAS Number	15548-39-7
3D model (JSmol)	Interactive image Interactive image
ChemSpider	9275088
PubChem CID	11099946
UNII	JSS99DM8F7
CompTox Dashboard (EPA)	DTXSID60455214
InChI InChI=1S/C12H22O11/c13-1-3-6(16)8(18)10(11(20)21-3)23-12-9(19)7(17)5(15)4(2-14)22-12/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8+,9+,10+,11?,12-/m1/s1Key: HIWPGCMGAMJNRG-VXSGSMIHSA-N InChI=1/C12H22O11/c13-1-3-6(16)8(18)10(11(20)21-3)23-12-9(19)7(17)5(15)4(2-14)22-12/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8+,9+,10+,11?,12-/m1/s1Key: HIWPGCMGAMJNRG-VXSGSMIHBW
SMILES OC1(O)(O)(O)(O(C(O)O(CO)2O)2O)O1 C(C1C(C(C(C(O1)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O
Properties
Chemical formula	C₁₂H₂₂O₁₁
Molar mass	342.30 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references

Chemical compound

2α-Mannobiose is a disaccharide. It is formed by a condensation reaction, when two mannose molecules react together, in the formation of a glycosidic bond.

References

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