Lanost-9(11)-en-18-oicacid, 3,12,20-trihydroxy-, g-lactone, (3b,12b)- (9CI)

Base Information

• Chemical Name: Lanost-9(11)-en-18-oicacid, 3,12,20-trihydroxy-, g-lactone, (3b,12b)- (9CI)
• CAS No.: 67797-17-5
• Molecular Formula: C₃₀H₄₈O₄
• Molecular Weight: 472.709
• Mol file: 67797-17-5.mol

Synonyms:1H,3H-Naphth[2',1':4,5]indeno[1,7a-c]furan,lanost-9(11)-en-18-oic acid deriv.; Isobivittogenin

Chemical Property of Lanost-9(11)-en-18-oicacid, 3,12,20-trihydroxy-, g-lactone, (3b,12b)- (9CI)

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Lanost-9(11)-en-18-oicacid, 3,12,20-trihydroxy-, g-lactone, (3b,12b)- (9CI)

There total 2 articles about Lanost-9(11)-en-18-oicacid, 3,12,20-trihydroxy-, g-lactone, (3b,12b)- (9CI) 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:

bivittoside A (77394-03-7) → D-Xylose (87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2) + 6-deoxy-D-glucose (488-79-9) + seychellogenin (24041-68-7) + (3S,3aS,5aS,5bS,9S,11aS,13R)-9,13-Dihydroxy-3,5a,8,8,11a-pentamethyl-3-(4-methyl-pentyl)-3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,13-tetradecahydro-3H-2-oxa-pentaleno[1,6a-a]phenanthren-1-one (67797-17-5,85054-54-2)

Guidance literature:

Further byproducts given; acidic hydrolysis;

DOI:10.1248/cpb.29.282

Reference yield:

bivittoside A (77394-03-7) → seychellogenin (24041-68-7) + isobivittogenin (67797-17-5)

Guidance literature:

With hydrogenchloride; In water; for 1h; Heating;

Reference yield:

isobivittogenin (67797-17-5) → seychellogenin (24041-68-7)

Guidance literature:

With acetyl chloride; In methanol; for 0.5h; Heating;

upstream raw materials:

bivittoside A

bivittoside A

Downstream raw materials:

seychellogenin