Emodin 6-O-|A-D-glucoside

Base Information

Chemical Name:Emodin 6-O-|A-D-glucoside
CAS No.:34298-85-6
Molecular Formula:C21H20O10
Molecular Weight:432.3775
Hs Code.:
Nikkaji Number:J269.602I
Wikidata:Q105269686
Metabolomics Workbench ID:142053
ChEMBL ID:CHEMBL522084

Synonyms:Emodin 6-O-|A-D-glucoside;CHEMBL522084;Glucoemodin;9,10-Anthracenedione, 3-(beta-D-glucopyranosyloxy)-1,8-dihydroxy-6-methyl-;Emodin-6-O-beta-D-glucopyranoside;Emodin 6-O-??-D-glucoside;Emodin 6-O-(c)micro-D-glucoside;HY-N8126;BDBM50025604;AKOS040763677;MS-27704;CS-0140173

Suppliers and Price of Emodin 6-O-|A-D-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 11 raw suppliers

Chemical Property of Emodin 6-O-|A-D-glucoside

Chemical Property:

Vapor Pressure:3.83E-27mmHg at 25°C
Melting Point:189 °C (methanol)
Boiling Point:801.9°Cat760mmHg
PKA:5.99±0.20(Predicted)
Flash Point:285.3°C
PSA：173.98000
Density:1.667g/cm³
LogP:-0.63970
XLogP3:0.9
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:3
Exact Mass:432.10564683
Heavy Atom Count:31
Complexity:700

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O
Isomeric SMILES:CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

Technology Process of Emodin 6-O-|A-D-glucoside

There total 3 articles about Emodin 6-O-|A-D-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: 71.0%

: 518-82-1
1,6,8-trihydroxy-3-methyl-9,10-anthraquinone

: 120221-14-9,119047-14-2
(2-chloro-4-nitrophenyl)-β-D-glucopyranoside

: 34298-85-6,86451-01-6
emodin-6-O-β-D-glucopyranoside

Guidance literature:: With recombinant Streptomyces venezuelae ISP₅₂₃₀ GT₁ Sv₀₁₈₉ glycosyltransferase; UDP; In aq. phosphate buffer; at 20 ℃; for 24h; pH=7.0; Enzymatic reaction;
DOI:10.1021/acs.joc.9b01130

Reference yield:

: 133-89-1
UDP-glucose

: 518-82-1
1,6,8-trihydroxy-3-methyl-9,10-anthraquinone

: 34298-85-6,86451-01-6
emodin-6-O-β-D-glucopyranoside

Guidance literature:: With glycosyltransferases YdhE bacillus licheniformi; magnesium chloride; In dimethyl sulfoxide; at 30 ℃; for 3h; pH=8.8; Enzymatic reaction;
DOI:10.1021/acs.orglett.9b03040