alpha-Hydrojuglone 4-glucoside

Base Information

Chemical Name:alpha-Hydrojuglone 4-glucoside
CAS No.:39015-63-9
Molecular Formula:C16H18O8
Molecular Weight:338.31
Hs Code.:
DSSTox Substance ID:DTXSID101310960
Nikkaji Number:J156.584B
Wikidata:Q105148915

Synonyms:alpha-Hydrojuglone 4-glucoside;39015-63-9;Compound NP-019140;SCHEMBL1628311;DTXSID101310960;AKOS040734962;NCGC00385147-01;1,4,8-Trihydroxynaphthalene 1-O-.beta.-D.-glucopyranoside;NCGC00385147-01_C16H18O8_beta-D-Glucopyranoside, 4,8-dihydroxy-1-naphthalenyl;(2S,3R,4S,5S,6R)-2-[(4,8-dihydroxy-1-naphthyl)oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

Suppliers and Price of alpha-Hydrojuglone 4-glucoside

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of alpha-Hydrojuglone 4-glucoside

Chemical Property:

Melting Point:178 °C (ethyl acetate)
PSA：139.84000
LogP:-0.57030
XLogP3:-0.4
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:338.10016753
Heavy Atom Count:24
Complexity:421

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC2=C(C=CC(=C2C(=C1)O)OC3C(C(C(C(O3)CO)O)O)O)O
Isomeric SMILES:C1=CC2=C(C=CC(=C2C(=C1)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O

Technology Process of alpha-Hydrojuglone 4-glucoside

There total 5 articles about alpha-Hydrojuglone 4-glucoside 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

: 39015-63-9
1,4,8-trihydroxynaphthalene-1-O-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: acetone; ethanolic KOH-solution

2: sodium acetate

3: ethanolic KOH-solution

With potassium hydroxide; sodium acetate; acetone;

Reference yield:

: (4,8-dihydroxy-[1]naphthyl)-(tetra-O-acetyl-β-D-glucopyranoside)

: 39015-63-9
1,4,8-trihydroxynaphthalene-1-O-β-D-glucopyranoside

Guidance literature:: With potassium hydroxide;

Reference yield:

: 6312-53-4
juglone

: 39015-63-9
1,4,8-trihydroxynaphthalene-1-O-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: acetone; ethanolic KOH-solution

2: sodium acetate

3: ethanolic KOH-solution

With potassium hydroxide; sodium acetate; acetone;