Olean-12-en-28-oicacid, 3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,(3b)-

Base Information

Chemical Name:Olean-12-en-28-oicacid, 3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,(3b)-
CAS No.:75799-17-6
Molecular Formula:C₄₆H₇₄O₁₅
Molecular Weight:867.085
Hs Code.:

Synonyms:Acanthopanaxsaponin CP3; CP3; Progenin; Prosapogenin CP3

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Olean-12-en-28-oicacid, 3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,(3b)-

Chemical Property:

Melting Point:219 - 221 °C
PSA：234.29000
LogP:3.01200

Purity/Quality:: 99% ^*data from raw suppliers

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Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

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Technology Process of Olean-12-en-28-oicacid, 3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,(3b)-

There total 10 articles about Olean-12-en-28-oicacid, 3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,(3b)- 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: 74.0%

: 1352410-47-9
benzyl oleanolate 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1 → 3)-2,4-di-O-acetyl-α-L-rhamnopyranosyl-(1 → 2)-α-L-arabinopyranoside

: 75799-18-7,96315-51-4,104494-26-0,142628-40-8,75799-17-6
oleanolic acid 3-O-3)-O-α-L-rhamnopyranosyl-(1->2)>-α-L-arabinopyranoside

Guidance literature:: benzyl oleanolate 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1 → 3)-2,4-di-O-acetyl-α-L-rhamnopyranosyl-(1 → 2)-α-L-arabinopyranoside; With palladium 10% on activated carbon; hydrogen; acetic acid; In methanol; dichloromethane; for 4h; under 760.051 Torr;

With sodium methylate; In methanol; dichloromethane; at 20 ℃; for 8h;
DOI:10.1016/j.ejmech.2013.04.016