117194-77-1 Usage
General Description
3A-AMINO-3A-DEOXY-(2AS,3AS)-BETA-CYCLODEXTRIN is a chemical compound that belongs to the family of cyclodextrins, which are cyclic oligosaccharides derived from starch. This specific compound has an amino group and a deoxy group attached to the beta-cyclodextrin structure, giving it unique properties and potential applications in various fields. It can be used as a chiral resolving agent, a drug delivery system, a stabilizer for flavors and fragrances, and in other pharmaceutical and chemical processes. Its structure allows it to form inclusion complexes with various guest molecules, enhancing their stability, solubility, and bioavailability. Overall, 3A-AMINO-3A-DEOXY-(2AS,3AS)-BETA-CYCLODEXTRIN is a versatile chemical compound with promising potential for various industrial and scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 117194-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,9 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117194-77:
(8*1)+(7*1)+(6*7)+(5*1)+(4*9)+(3*4)+(2*7)+(1*7)=131
131 % 10 = 1
So 117194-77-1 is a valid CAS Registry Number.
InChI:InChI=1/C42H71NO34/c43-15-16(51)36-64-8(1-44)29(15)71-37-23(58)17(52)31(10(3-46)65-37)73-39-25(60)19(54)33(12(5-48)67-39)75-41-27(62)21(56)35(14(7-50)69-41)77-42-28(63)22(57)34(13(6-49)70-42)76-40-26(61)20(55)32(11(4-47)68-40)74-38-24(59)18(53)30(72-36)9(2-45)66-38/h8-42,44-63H,1-7,43H2/t8-,9-,10-,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-/m1/s1
117194-77-1Relevant articles and documents
Functionalization of Cyclodextrins via Reactions of 2,3-Anhydrocyclodextrins
Yuan, De-Qi,Tahara, Tsutomu,Chen, Wen-Hua,Okabe, Yuji,Yang, Cheng,Yagi, Youichi,Nogami, Yasuyoshi,Fukudome, Makoto,Fujita, Kahee
, p. 9456 - 9466 (2003)
Three types of reactions of 2,3-anhydro-β-cyclodextrins, namely nucleophilic ring-opening, reduction to 2-enopyranose, and reduction to 3-deoxypyranose, have been investigated to regio- and stereoselectively functionalize the secondary face of β-cyclodext
