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PHENYL-O-(4-O-ACETYL-2,3,6-TRI-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL)-(1->4)-O-(2,3,6-TRI-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL)-(1->4)-2,3,6-TRI-O-BENZYL-1-T
SpectraBase Compound ID 1p4vDHcBXse
InChI InChI=1S/C89H92O16S/c1-64(90)100-78-75(61-91-52-65-32-12-2-13-33-65)101-87(84(97-58-71-44-24-8-25-45-71)81(78)94-55-68-38-18-5-19-39-68)104-79-76(62-92-53-66-34-14-3-15-35-66)102-88(85(98-59-72-46-26-9-27-47-72)82(79)95-56-69-40-20-6-21-41-69)105-80-77(63-93-54-67-36-16-4-17-37-67)103-89(106-74-50-30-11-31-51-74)86(99-60-73-48-28-10-29-49-73)83(80)96-57-70-42-22-7-23-43-70/h2-51,75-89H,52-63H2,1H3/t75-,76-,77-,78-,79-,80-,81+,82+,83+,84-,85-,86-,87-,88-,89+/m1/s1
InChIKey MUCQYPFWDAJDDE-HNHAVOSASA-N
Mol Weight 1449.8 g/mol
Molecular Formula C89H92O16S
Exact Mass 1448.610608 g/mol
Enantiomer InChIKey MUCQYPFWDAJDDE-KTPBDUGDSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Title Journal or Book Year
Chemical synthesis of 6‴-α-maltotriosyl-maltohexaose as substrate for enzymes in starch biosynthesis and degradation Carbohydrate Research 1999

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