urolithin M7

Base Information

Chemical Name:urolithin M7
CAS No.:531512-26-2
Molecular Formula:C₁₃H₈O₅
Molecular Weight:244.204
Hs Code.:

Synonyms:

Suppliers and Price of urolithin M7

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

TRC
UrolithinM7
10mg
$ 275.00

Total 1 raw suppliers

Chemical Property of urolithin M7

Chemical Property:

Melting Point:>300 °C
Boiling Point:583.0±29.0 °C(Predicted)
Density:1.640±0.06 g/cm3(Predicted)

Purity/Quality:

97% ^*data from raw suppliers

UrolithinM7 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Urolithin M7 is an intestinal microbial metabolite of ellagitannins.

Technology Process of urolithin M7

There total 13 articles about urolithin M7 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: 98.0%

: 1346113-32-3
8-acetoxy-3,10-dimethoxy-6H-dibenzo[b,d]pyran-6-one

: 531512-26-2
urolithin M7

Guidance literature:: With hydrogen iodide; In water; at 127 ℃; for 0.5h;
DOI:10.1055/s-0030-1261203

Reference yield: 94.0%

: 3,8,10-trimethoxy-6H-benzo[c]chromen-6-one

: 531512-26-2
urolithin M7

Guidance literature:: With boron tribromide; In dichloromethane; at -78 - 20 ℃; for 72h;
DOI:10.1021/acs.joc.7b00256

Reference yield:

: 673-22-3
2-Hydroxy-4-methoxybenzaldehyde

: 531512-26-2
urolithin M7

Guidance literature:: Multi-step reaction with 7 steps

1.1: piperidine / benzene / 3 h / Reflux; azeotropic removal of water

2.1: water; benzene / 168 h / 80 °C / Inert atmosphere

3.1: sodium hydroxide / ethanol; water / 1 h / 100 °C

4.1: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C / Inert atmosphere

4.2: 12 h / Reflux; Inert atmosphere

5.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran; hexanes / 96 h / 0 - 20 °C / Inert atmosphere

6.1: 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid / dichloromethane / 96 h / 20 °C

7.1: hydrogen iodide / water / 0.5 h / 127 °C

With piperidine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; hydrogen iodide; sodium hydride; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; hexanes; ethanol; dichloromethane; water; mineral oil; benzene; 2.1: inverse electron-demand Diels-Alder (IEDDA) reaction / 6.1: Baeyer-Villiger oxidation;
DOI:10.1055/s-0030-1261203