cis-3,5,3',4'-Tetrahydroxystilbene

Base Information Edit

Chemical Name:cis-3,5,3',4'-Tetrahydroxystilbene
CAS No.:106325-86-4
Molecular Formula:C14H12O4
Molecular Weight:244.24300
Hs Code.:
DSSTox Substance ID:DTXSID40424968
Nikkaji Number:J2.511.111G
Wikidata:Q27145793
Metabolomics Workbench ID:123698
ChEMBL ID:CHEMBL1603409
Mol file:106325-86-4.mol

Synonyms:cis-Piceatannol;106325-86-4;cis-3,5,3',4'-tetrahydroxystilbene;4-[(Z)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,2-diol;CHEBI:76156;Lopac-P-0453;CHEMBL1603409;SCHEMBL19953785;DTXSID40424968;CDRPUGZCRXZLFL-UPHRSURJSA-N;(Z)-3,5,3',4'-tetrahydroxystilbene;NCGC00015794-01;(Z)-3,5,3/',4/'-Tetrahydroxystilbene;J-001574;Q27145793;5-[(1Z)-2-(3,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol

Suppliers and Price of cis-3,5,3',4'-Tetrahydroxystilbene

Supply Marketing:Edit

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

TRC
cis-Piceatannol
50mg
$ 1455.00

Total 3 raw suppliers

Chemical Property of cis-3,5,3',4'-Tetrahydroxystilbene Edit

Chemical Property:

Melting Point:216-218°C (dec.)
PSA：80.92000
LogP:2.67940
Storage Temp.:Refrigerator, Under Inert Atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:2.9
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:244.07355886
Heavy Atom Count:18
Complexity:282

Purity/Quality:

97% ^*data from raw suppliers

cis-Piceatannol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O
Isomeric SMILES:C1=CC(=C(C=C1/C=C\C2=CC(=CC(=C2)O)O)O)O
Uses The cis isomer of human metabolite of Resveratrol (R150000).

Technology Process of cis-3,5,3',4'-Tetrahydroxystilbene

There total 59 articles about cis-3,5,3',4'-Tetrahydroxystilbene 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: 100.0%

: 501-36-0
(E)-5-[2-4-(hydroxyphenyl)ethenyl]-1,3-benzenediol

: 10083-24-6,106325-86-4
trans-piceatannol

Guidance literature:: With streptomyces avermilitis tyrosinase; benzene-1,2-diol; In aq. buffer; for 3h; pH=8; Reagent/catalyst; Enzymatic reaction;

Reference yield: 91.0%

: 1018449-53-0
3',4'-bis(tert-butyldimethylsiloxy)-3,5-dihydroxystilbene

: 10083-24-6,106325-86-4
trans-piceatannol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 0.0833333h;
DOI:10.1071/CH07044

Reference yield: 90.0%

: 83088-26-0
(E)-tetramethylpiceatannol

: 10083-24-6,106325-86-4
trans-piceatannol

Guidance literature:: With boron tribromide; In dichloromethane; at -30 - 20 ℃; for 4h; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.orglett.0c02236