Oleanolic acid base + O-HexA-Hex

Base Information

• Chemical Name: Oleanolic acid base + O-HexA-Hex
• CAS No.: 25406-56-8
• Molecular Formula: C42H66 O14
• Molecular Weight: 794.978
• Wikidata: Q104944506
• Mol file: 25406-56-8.mol

Synonyms:Oleanolic acid base + O-HexA-Hex

Chemical Property of Oleanolic acid base + O-HexA-Hex

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 248-250 °C
• Boiling Point: 920.3°Cat760mmHg
• PKA: 2.75±0.70(Predicted)
• Flash Point: 271.6°C
• PSA: 232.90000
• Density: 1.37g/cm³
• LogP: 2.97430
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 14
• Rotatable Bond Count: 7
• Exact Mass: 794.44525677
• Heavy Atom Count: 56
• Complexity: 1560

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C

Technology Process of Oleanolic acid base + O-HexA-Hex

There total 4 articles about Oleanolic acid base + O-HexA-Hex which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3-O-{[β-D-glucopyranosyl (1->2)]-[α-L-arabinopyranosyl (1->3)]-β-D-glucuronopyranosyl}oleanolic acid (121521-92-4) → 3-O-3)-O-(β-D-glucopyranosyluronsaeure)>-oleanolsaeure (25406-56-8,26020-15-5) + calenduloside E (26020-14-4,108322-31-2)

Guidance literature:

With sulfuric acid; at 70 ℃; for 16h; Yield given. Yields of byproduct given;

Reference yield:

28-(β-D-Glucopyranosyloxy)-28-oxoolean-12-en-3β-yl 3-O-(β-D-glucopyranosyl)-β-D-glucopyranosiduronic acid → 3-O-3)-O-(β-D-glucopyranosyluronsaeure)>-oleanolsaeure (25406-56-8,26020-15-5)

Guidance literature:

With potassium hydroxide; for 1h; Yield given; Heating;

DOI:10.1002/ardp.19873200211

Reference yield:

28-(β-D-Glucopyranosyloxy)-28-oxoolean-12-en-3β-yl 3-O-(β-D-glucopyranosyl)-β-D-glucopyranosiduronic acid → 3-O-3)-O-(β-D-glucopyranosyluronsaeure)>-oleanolsaeure (25406-56-8,26020-15-5) + calenduloside E (26020-14-4,108322-31-2)

Guidance literature:

With 1,4-dioxane; hydrogenchloride; for 0.166667h; Heating;

DOI:10.1002/ardp.19873200211

upstream raw materials:

3-O-{[β-D-glucopyranosyl (1->2)]-[α-L-arabinopyranosyl (1->3)]-β-D-glucuronopyranosyl}oleanolic acid

kalopanax-saponin F (3-O-α-arabinopyranosyl-(1->2)-<β-glucopyranosyl-(1->3)>-β-glucuronopyranosyl oleanolic acid 28-O-β-glucopyranosyl ester

Downstream raw materials:

D-Glucose

D-glucuronic acid

Oleanolic acid

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