(20S)-3β-[2-O-(6-Deoxy-β-D-glucopyranosyl)-β-D-xylopyranosyloxy]-12α,20-dihydroxy-5α-lanost-9(11)-en-18-oic acid 18,20-lactone

Base Information Edit

Chemical Name:(20S)-3β-[2-O-(6-Deoxy-β-D-glucopyranosyl)-β-D-xylopyranosyloxy]-12α,20-dihydroxy-5α-lanost-9(11)-en-18-oic acid 18,20-lactone
CAS No.:77394-03-7
Molecular Formula:C41H66O12
Molecular Weight:750.968
Hs Code.:
Mol file:77394-03-7.mol

Synonyms:bivittoside A;

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

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Chemical Property of (20S)-3β-[2-O-(6-Deoxy-β-D-glucopyranosyl)-β-D-xylopyranosyloxy]-12α,20-dihydroxy-5α-lanost-9(11)-en-18-oic acid 18,20-lactone Edit

Chemical Property:

Vapor Pressure:1.97E-34mmHg at 25°C
Boiling Point:859.6°Cat760mmHg
Flash Point:254.2°C
PSA：184.60000
Density:1.29g/cm³
LogP:3.36030

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (20S)-3β-[2-O-(6-Deoxy-β-D-glucopyranosyl)-β-D-xylopyranosyloxy]-12α,20-dihydroxy-5α-lanost-9(11)-en-18-oic acid 18,20-lactone

There total 4 articles about (20S)-3β-[2-O-(6-Deoxy-β-D-glucopyranosyl)-β-D-xylopyranosyloxy]-12α,20-dihydroxy-5α-lanost-9(11)-en-18-oic acid 18,20-lactone 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:

: 77394-04-8
bivittoside B

: 77394-03-7
bivittoside A

Guidance literature:: With sodium acetate; In acetic acid; at 38 ℃; for 120h; hesperidinase, pH=5.0;

Reference yield:

: 122456-69-3
C₄₁H₆₄O₁₂

: 77394-03-7
bivittoside A

Guidance literature:: Raney Ni(W-2); In ethanol; for 5h; Yield given; Heating;

Reference yield:

: 122476-95-3
DS-pervicoside B

: 77394-03-7
bivittoside A

Guidance literature:: Multi-step reaction with 2 steps

1: 7 h / 35 °C / hesperidinase, AcONa-AcOH buffer

2: Raney Ni(W-2) / ethanol / 5 h / Heating

Raney Ni(W-2); In ethanol;