Thymusin

Base Information

Chemical Name:Thymusin
CAS No.:76844-66-1
Molecular Formula:C17H14O7
Molecular Weight:330.294
Hs Code.:
DSSTox Substance ID:DTXSID501319152
Nikkaji Number:J489.560F
Wikidata:Q104252889
Metabolomics Workbench ID:24528
ChEMBL ID:CHEMBL478426

Synonyms:Thymusin;5,6,4'-Trihydroxy-7,8-dimethoxyflavone;CHEMBL478426;DTXSID501319152;BDBM50412277;LMPK12111445;5,6-Dihydroxy-2-(4-hydroxyphenyl)-7,8-dimethoxy-4H-chromen-4-one #;76844-66-1

Suppliers and Price of Thymusin

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 0 raw suppliers

Chemical Property of Thymusin

Chemical Property:

Melting Point:230 °C
Boiling Point:653.4±55.0 °C(Predicted)
PSA：109.36000
Density:1.483±0.06 g/cm3(Predicted)
LogP:2.59400
XLogP3:2.6
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:3
Exact Mass:330.07395278
Heavy Atom Count:24
Complexity:497

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=C2C(=O)C=C(OC2=C1OC)C3=CC=C(C=C3)O)O)O

Technology Process of Thymusin

There total 6 articles about Thymusin 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: 5.0%

: 16545-23-6
xanthomicrol

: 76844-66-1
5,6,4′-trihydroxy-7,8-dimethoxy flavone

Guidance literature:: With hydrogenchloride; In methanol; water; at 100 ℃; for 48h;
DOI:10.1016/S0040-4020(01)91379-1

Reference yield:

: 76844-59-2
6,4'-dibenzyloxy-5,7,8-trimethoxyflavone

: 76844-66-1
5,6,4′-trihydroxy-7,8-dimethoxy flavone

Guidance literature:: With aluminium trichloride; In acetonitrile; for 4h; Heating;

Reference yield:

: 4397-53-9
p-benzyloxybenzaldehyde

: 76844-66-1
5,6,4′-trihydroxy-7,8-dimethoxy flavone

Guidance literature:: Multi-step reaction with 3 steps

1: 0.6 g / aq. KOH / ethanol / 48 h / Ambient temperature

2: 0.7 g / SeO₂ / 3-methyl-butan-1-ol / 72 h / Heating

3: 0.19 g / AlCl₃ / acetonitrile / 4 h / Heating

With potassium hydroxide; aluminium trichloride; selenium(IV) oxide; In ethanol; i-Amyl alcohol; acetonitrile;