Welcome to LookChem.com Sign In|Join Free
  • or
Z-12β-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyloxy)-3α-hydroxydammar-20(22)-en-24-one is a complex organic compound with a molecular formula of C41H56O10. It is a triterpenoid glycoside, which is a type of natural product derived from plants, characterized by the presence of a dammarane skeleton and a glucose moiety. The compound features a 3α-hydroxydammarane core with a 20(22)-en-24-one functional group, indicating the presence of a double bond at the 20(22) position and a ketone group at the 24 position. The glucose unit is attached to the 12β position of the dammarane core and is acetylated at the 2', 3', 4', and 6' positions, which means that these hydroxyl groups are esterified with acetic acid. Z-12β-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyloxy)-3α-hydroxydammar-20(22)-en-24-one is of interest in the field of natural product chemistry and may have potential applications in pharmaceutical or chemical research due to its unique structure and the biological activities often associated with triterpenoid glycosides.

88109-93-7

Post Buying Request

88109-93-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

88109-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88109-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,0 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88109-93:
(7*8)+(6*8)+(5*1)+(4*0)+(3*9)+(2*9)+(1*3)=157
157 % 10 = 7
So 88109-93-7 is a valid CAS Registry Number.

88109-93-7Downstream Products

88109-93-7Relevant academic research and scientific papers

REGIO- AND STEREOSELECTIVE GLYCOSYLATION OF 20(S),24(R)-EPOXYDAMMARANE-3,12β,25-TRIOLS WITH CHOLESTERYL (α-D-GLUCOSE ORTHOACETATE). III.

Samoshina, N. F.,Novikov, V. L.,Denisenko, V. A.,Uvarova, N. I.

, p. 299 - 304 (1983)

The glycosylation of 20(S),24(R)-epoxydammarane-3,124b,25-triols under the conditions of the previous formation of an ion pair with a Lewis acid and subsequent treatment with cholesteryl (α-D-glucose orthoacetate) leads to the selective formation with high yields of the corresponding 12-monoglucosides having the trans configuration of the glucosidic bond.The regioselectivity of the direct glycosylation of 20(S),24(R)-epoxydammarane-3,12β,25-triols by orthoesters is determined by the influence of intramolecular hydrogen bonds in the initial triols.Details of the PMRand 13C NMR spectra of the new compounds obtained are given.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 88109-93-7