Urolithin D

Base Information

Chemical Name:Urolithin D
CAS No.:131086-98-1
Molecular Formula:C13H8O6
Molecular Weight:260.199
Hs Code.:
UNII:JVT9VXW2DJ
DSSTox Substance ID:DTXSID70156886
Nikkaji Number:J403.505D
Wikidata:Q83025003
Pharos Ligand ID:AYNF3LWRFN2T
ChEMBL ID:CHEMBL6338
Mol file:131086-98-1.mol

Synonyms:urolithin D

Suppliers and Price of Urolithin D

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

Usbiological
Urolithin D
5mg
$ 446.00

TRC
UrolithinD
5mg
$ 175.00

Medical Isotopes, Inc.
UrolithinD
250 mg
$ 2120.00

American Custom Chemicals Corporation
3,4,8,9-TETRAHYDROXY-6H-DIBENZO[B,D]PYRAN-6-ONE 95.00%
100MG
$ 6825.00

American Custom Chemicals Corporation
3,4,8,9-TETRAHYDROXY-6H-DIBENZO[B,D]PYRAN-6-ONE 95.00%
10MG
$ 1312.50

American Custom Chemicals Corporation
3,4,8,9-TETRAHYDROXY-6H-DIBENZO[B,D]PYRAN-6-ONE 95.00%
5MG
$ 501.73

Total 13 raw suppliers

Chemical Property of Urolithin D

Chemical Property:

Vapor Pressure:1.13E-16mmHg at 25°C
Melting Point:>260°C (dec.)
Boiling Point:634.1°Cat760mmHg
Flash Point:253°C
PSA：111.13000
Density:1.766g/cm³
LogP:1.76860
Storage Temp.:Hygroscopic, Refrigerator, under inert atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:1.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:0
Exact Mass:260.03208797
Heavy Atom Count:19
Complexity:372

Purity/Quality:

97% ^*data from raw suppliers

Urolithin D ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C2=C1C3=CC(=C(C=C3C(=O)O2)O)O)O)O
Uses Urolithin D is used in biological studies to evaluate DNA gyrase inhibitory activity of ellagic acid derivatives.

Technology Process of Urolithin D

There total 10 articles about Urolithin D 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:

: 146776-39-8
3,4,8,9-Tetramethoxy-benzo[c]chromen-6-one

: 131086-98-1
urolithin D

Guidance literature:: With boron tribromide; In dichloromethane;
DOI:10.1016/S0960-894X(97)10197-4

Reference yield:

: 118062-05-8
2,3,4-trimethoxyphenylboronic acid

: 131086-98-1
urolithin D

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / 2 M aq.Na₂CO₃ / Pd(PPh₃)4 / 1,2-dimethoxy-ethane; ethanol / 18 h / Heating

2: 1) BBr₃, 2) glacial HOAc / 1) CH₂Cl₂, overnight, 2) reflux, 18 h

With boron tribromide; sodium carbonate; acetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; ethanol;
DOI:10.1021/jo00012a004

Reference yield:

: 105875-33-0
2-bromo-N,N-diethyl-4,5-dimethoxy-benzamide

: 131086-98-1
urolithin D

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / 2 M aq.Na₂CO₃ / Pd(PPh₃)4 / 1,2-dimethoxy-ethane; ethanol / 18 h / Heating

2: 1) BBr₃, 2) glacial HOAc / 1) CH₂Cl₂, overnight, 2) reflux, 18 h

With boron tribromide; sodium carbonate; acetic acid; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; ethanol;
DOI:10.1021/jo00012a004