Cas no 85220-53-7 (CYCLODEXTRIN)

CYCLODEXTRIN structure
CYCLODEXTRIN structure
Product Name:CYCLODEXTRIN
CAS No:85220-53-7
MF:C54H90O45
MW:1459.26542329788
CID:2692721
Update Time:2024-01-03

CYCLODEXTRIN Chemical and Physical Properties

Names and Identifiers

    • CYCLODEXTRIN
    • Heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-&beta
    • Di-O-methyl-&beta
    • Heptakis(2,3-dimethyl)-&beta
    • Heptakis-(6-O-tert-butyldimethylsilyl)-&beta
    • Heptakis(6-bromo-6-deoxy)-&beta
    • Heptakis(2,3-di-O-acetyl)-&beta
    • 6A,6B,6C,6D,6E,6F,6G-Heptakis-O-(2-hydroxypropyl)-&beta
    • 2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39,42,44-Octadecaoxadecacyclo[41.2.2.23,6.28,11.213,16.218,21.223,26.228,31.233,36.238,41]trihexacontane, δ-cyclodextrin deriv. (ZCI)
    • Cyclomaltononaose
    • Stereoisomer of 5,10,15,20,25,30,35,40,45-nonakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39,42,44-octadecaoxadecacyclo[41.2.2.23,6.28,11.213,16.218,21.223,26.228,31.233,36.238,41]trihexacontane-46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63-octadecol
    • Inchi： 1S/C54H90O45/c55-1-10-37-19(64)28(73)46(82-10)92-38-11(2-56)84-48(30(75)21(38)66)94-40-13(4-58)86-50(32(77)23(40)68)96-42-15(6-60)88-52(34(79)25(42)70)98-44-17(8-62)90-54(36(81)27(44)72)99-45-18(9-63)89-53(35(80)26(45)71)97-43-16(7-61)87-51(33(78)24(43)69)95-41-14(5-59)85-49(31(76)22(41)67)93-39-12(3-57)83-47(91-37)29(74)20(39)65/h10-81H,1-9H2/t10-,11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27+,28-,29-,30-,31-,32-,33-,34-,35-,36+,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48-,49-,50-,51-,52-,53-,54-/m1/s1
    • InChI Key： UXRSQEDGDSCMFT-LYTANOLKSA-N
    • SMILES： C([C@H]1O[C@@H]2O[C@H]3[C@H](O)[C@@H](O)[C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@@H](O[C@@H]7[C@@H](CO)O[C@H](O[C@@H]8[C@@H](CO)O[C@H](O[C@@H]9[C@@H](CO)O[C@H](O[C@@H]%10[C@@H](CO)O[C@H](O[C@H]1[C@H]([C@@H]2O)O)[C@H](O)[C@H]%10O)[C@H](O)[C@H]9O)[C@H](O)[C@H]8O)[C@H](O)[C@H]7O)O[C@@H]6CO)O[C@@H]5CO)O[C@@H]4CO)O[C@@H]3CO)O

CYCLODEXTRIN Production Method

Production Method 1

Reaction Conditions
1.1 Catalysts: Cyclodextrin glucanotransferase Solvents: Water ;  240 min, pH 5.5, 60 °C; 10 min, reflux
Reference
Effect of the reaction temperature on the transglycosylation reactions catalyzed by the cyclodextrin glucanotransferase from Bacillus macerans for the synthesis of large-ring cyclodextrins
Qi, Qingsheng; She, Xiaoyan; Endo, Tomohiro; Zimmermann, Wolfgang, Tetrahedron, 2004, 60(3), 799-806

CYCLODEXTRIN Raw materials

CYCLODEXTRIN Preparation Products

CYCLODEXTRIN Related Literature

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