quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside

Base Information

Chemical Name:quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside
CAS No.:86749-52-2
Molecular Formula:C₂₆H₂₈O₁₅
Molecular Weight:580.499
Hs Code.:

Synonyms:

Suppliers and Price of quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside

There total 11 articles about quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside 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:

: 1332699-63-4
C₃₆H₃₈O₂₀

: 86749-52-2
quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside

Guidance literature:: With sodium methylate; In methanol; at 20 ℃; for 3h;
DOI:10.1021/np200444n

Reference yield:

: 1350770-01-2
C₂₁H₃₀O₁₄

: 86749-52-2
quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen bromide; acetic acid / chloroform / 0 °C

2: benzyltriethylammonium bromide; potassium hydroxide / chloroform; water / 15 h / Reflux

3: palladium on activated charcoal; hydrogen / methanol / 4 h / 20 °C / 760.05 Torr

4: sodium methylate / methanol / 3 h / 20 °C

With palladium on activated charcoal; hydrogen bromide; hydrogen; sodium methylate; benzyltriethylammonium bromide; acetic acid; potassium hydroxide; In methanol; chloroform; water; 4: Zemplen deacetylation;
DOI:10.1021/np200444n

Reference yield:

: 39524-38-4
2,3,4-tri-O-acetyl-6-deoxy-beta-L-mannopyranosyl bromide

: 86749-52-2
quercetin 3-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside

Guidance literature:: Multi-step reaction with 8 steps

1: mercury(II) cyanide / nitromethane; benzene / 2 h / 20 °C

2: sulfuric acid; water / acetone / 2 h / Reflux

3: pyridine / 24 h / 20 °C

4: palladium on activated charcoal; hydrogen

5: hydrogen bromide; acetic acid / chloroform / 0 °C

6: benzyltriethylammonium bromide; potassium hydroxide / chloroform; water / 15 h / Reflux

7: palladium on activated charcoal; hydrogen / methanol / 4 h / 20 °C / 760.05 Torr

8: sodium methylate / methanol / 3 h / 20 °C

With pyridine; sulfuric acid; palladium on activated charcoal; water; hydrogen bromide; hydrogen; sodium methylate; benzyltriethylammonium bromide; mercury(II) cyanide; acetic acid; potassium hydroxide; In methanol; nitromethane; chloroform; water; acetone; benzene; 8: Zemplen deacetylation;
DOI:10.1021/np200444n