(E)-8-(2,5-Dimethylstyryl)-1,3-diethyl-7-methylxanthine

Base Information

Chemical Name:(E)-8-(2,5-Dimethylstyryl)-1,3-diethyl-7-methylxanthine
CAS No.:155271-27-5
Molecular Formula:C₂₀H₂₄N₄O₂
Molecular Weight:352.436
Hs Code.:
Wikidata:Q76389383

Synonyms:(E)-8-(2,5-Dimethylstyryl)-1,3-diethyl-7-methylxanthine;155271-27-5;(E)-1,3-Diethyl-8-(2-(2,5-dimethylphenyl)ethenyl)-7-methyl-3,7-dihydro-1H-purine-2,6-dione;1H-Purine-2,6-dione, 3,7-dihydro-1,3-diethyl-8-(2-(2,5-dimethylphenyl)ethenyl)-7-methyl-, (E)-;SCHEMBL7315044;SCHEMBL7315051;LS-126717

Suppliers and Price of (E)-8-(2,5-Dimethylstyryl)-1,3-diethyl-7-methylxanthine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (E)-8-(2,5-Dimethylstyryl)-1,3-diethyl-7-methylxanthine

Chemical Property:

Vapor Pressure:1.94E-12mmHg at 25°C
Boiling Point:556.9°Cat760mmHg
Flash Point:290.6°C
Density:1.18g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:352.18992602
Heavy Atom Count:26
Complexity:578

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN1C2=C(C(=O)N(C1=O)CC)N(C(=N2)C=CC3=C(C=CC(=C3)C)C)C
Isomeric SMILES:CCN1C2=C(C(=O)N(C1=O)CC)N(C(=N2)/C=C/C3=C(C=CC(=C3)C)C)C

Technology Process of (E)-8-(2,5-Dimethylstyryl)-1,3-diethyl-7-methylxanthine

There total 3 articles about (E)-8-(2,5-Dimethylstyryl)-1,3-diethyl-7-methylxanthine 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: 62.0%