quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside

Base Information

Chemical Name:quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside
CAS No.:159030-04-3
Molecular Formula:C₂₆H₂₈O₁₆
Molecular Weight:596.499
Hs Code.:

Synonyms:quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside

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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 quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside

Chemical Property:

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Technology Process of quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside

There total 14 articles about quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside 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:

: 572-09-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 159030-04-3
quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 18 percent / mercuric cyanide, mercuric bromide / acetonitrile / 24 h

2: HBr, AcOH / CHCl₃; acetic acid / 3 h / 0 °C

3: benzyltriethylammonium bromide, 1.25M aq. KOH / CHCl₃ / 15 h / Heating

4: H₂ / 10percent Pd/C / methanol / 4 h / 20 °C / 760 Torr

5: NaOMe / methanol / 3 h / 20 °C

With potassium hydroxide; hydrogen bromide; hydrogen; sodium methylate; mercury(II) cyanide; benzyltriethylammonium bromide; acetic acid; mercury dibromide; palladium on activated charcoal; In methanol; chloroform; acetic acid; acetonitrile;

Reference yield:

: 159067-20-6
Acetic acid (2S,3R,4S,5R)-5-acetoxy-2-[2-(3,4-dihydroxy-phenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yloxy]-3-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

: 159030-04-3
quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside

Guidance literature:: With sodium methylate; In methanol; at 20 ℃; for 3h; Yield given;

Reference yield:

: 19186-38-0
O¹,O³,O⁴-Triacetyl-α-D-xylopyranose

: 159030-04-3
quercetin-3-O-β-D-glucopyranosyl-(1<*>2)-β-D-xylopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 18 percent / mercuric cyanide, mercuric bromide / acetonitrile / 24 h

2: HBr, AcOH / CHCl₃; acetic acid / 3 h / 0 °C

3: benzyltriethylammonium bromide, 1.25M aq. KOH / CHCl₃ / 15 h / Heating

4: H₂ / 10percent Pd/C / methanol / 4 h / 20 °C / 760 Torr

5: NaOMe / methanol / 3 h / 20 °C

With potassium hydroxide; hydrogen bromide; hydrogen; sodium methylate; mercury(II) cyanide; benzyltriethylammonium bromide; acetic acid; mercury dibromide; palladium on activated charcoal; In methanol; chloroform; acetic acid; acetonitrile;