Cas no 146713-88-4 (Urs-12-en-28-oic acid, 3-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl)oxy]-19-hydroxy-, β-D-glucopyranosyl ester, (3β)- (9CI))
![Urs-12-en-28-oic acid, 3-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl)oxy]-19-hydroxy-, β-D-glucopyranosyl ester, (3β)- (9CI) structure](https://ossimg.kuujia.com/scimg/147000/146713-88-4x500.png)
146713-88-4 structure
Product Name:Urs-12-en-28-oic acid, 3-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl)oxy]-19-hydroxy-, β-D-glucopyranosyl ester, (3β)- (9CI)
CAS No:146713-88-4
MF:C53H86O23
MW:1091.23615980148
CID:154432
Update Time:2024-03-01
Urs-12-en-28-oic acid, 3-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl)oxy]-19-hydroxy-, β-D-glucopyranosyl ester, (3β)- (9CI) Chemical and Physical Properties
Names and Identifiers
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- IlexosideXVIII
- 3)]-a-L-arabinopyranosyl)oxy]-19-hydroxy-, b-D-glucopyranosyl ester, (3b)- (9CI)
- Urs-12-en-28-oic acid, 3-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl)oxy]-19-hydroxy-, β-D-glucopyranosyl ester, (3β)- (9CI)
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- Inchi： 1S/C53H86O23/c1-22-10-15-53(47(67)76-45-39(66)36(63)33(60)27(20-56)72-45)17-16-50(5)23(42(53)52(22,7)68)8-9-29-49(4)13-12-30(48(2,3)28(49)11-14-51(29,50)6)73-46-41(75-44-38(65)35(62)32(59)26(19-55)71-44)40(24(57)21-69-46)74-43-37(64)34(61)31(58)25(18-54)70-43/h8,22,24-46,54-66,68H,9-21H2,1-7H3
- InChI Key： JAWUKHLXDDSSKK-UHFFFAOYSA-N
- SMILES： CC1C(O)(C)C2C(C(OC3C(O)C(O)C(O)C(CO)O3)=O)(CCC3(C4(C(C5(C(CC4)C(C)(C)C(OC4C(OC6C(O)C(O)C(O)C(CO)O6)C(OC6C(O)C(O)C(O)C(CO)O6)C(O)CO4)CC5)C)CC=C32)C)C)CC1
Urs-12-en-28-oic acid, 3-[(O-β-D-glucopyranosyl-(1→2)-O-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl)oxy]-19-hydroxy-, β-D-glucopyranosyl ester, (3β)- (9CI) Related Literature
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Bruce Parkinson Energy Environ. Sci., 2010,3, 509-511
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Daniel Messmer,Stefan Salentinig,Jakob Heier Nanoscale, 2019,11, 6929-6938
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Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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