2,4(1H,3H)-Pyrimidinedione, 5-iodo-1,3-bis(phenylmethyl)-

Base Information

Chemical Name:2,4(1H,3H)-Pyrimidinedione, 5-iodo-1,3-bis(phenylmethyl)-
CAS No.:119125-40-5
Molecular Formula:C18H15IN2O2
Molecular Weight:418.234
Hs Code.:
DSSTox Substance ID:DTXSID20425079
Nikkaji Number:J465.500A
Wikidata:Q82237835
Mol file:119125-40-5.mol

Synonyms:1,3-dibenzyl-5-iodouracil;119125-40-5;ChemDiv3_002099;2,4(1H,3H)-Pyrimidinedione, 5-iodo-1,3-bis(phenylmethyl)-;Oprea1_058759;SCHEMBL5796829;DTXSID20425079;HMS1478P09;IDI1_021065;EU-0040407;10.14272/FPEITTIRQBXGLZ-UHFFFAOYSA-N.1;SR-01000453416;1,3-dibenzyl-5-iodopyrimidine-2,4(1H,3H)-dione;doi:10.14272/FPEITTIRQBXGLZ-UHFFFAOYSA-N.1;SR-01000453416-1;BRD-K60764527-001-01-5

Suppliers and Price of 2,4(1H,3H)-Pyrimidinedione, 5-iodo-1,3-bis(phenylmethyl)-

Supply Marketing:

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

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Chemical Property of 2,4(1H,3H)-Pyrimidinedione, 5-iodo-1,3-bis(phenylmethyl)-

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:418.01783
Heavy Atom Count:23
Complexity:479

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN2C=C(C(=O)N(C2=O)CC3=CC=CC=C3)I

Technology Process of 2,4(1H,3H)-Pyrimidinedione, 5-iodo-1,3-bis(phenylmethyl)-

There total 3 articles about 2,4(1H,3H)-Pyrimidinedione, 5-iodo-1,3-bis(phenylmethyl)- 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: 87.0%

: 34001-56-4
1,3-dibenzyluracil

: 119125-40-5
1,3-dibenzyl-5-iodouracil

Guidance literature:: With N-iodo-succinimide; trifluoroacetic acid; trifluoroacetic anhydride; for 1h; Heating;

Reference yield:

: 100-39-0
benzyl bromide

: 696-07-1
5-iodouracil

: 119125-40-5
1,3-dibenzyl-5-iodouracil

: 153865-87-3
1-benzyl-5-iodo-1,2,3,4-tetrahydropyrimidine-2,4-dione

Guidance literature:: With potassium carbonate; Yield given. Multistep reaction. Yields of byproduct given; 1) DMF, 2 d, room temperature; 2) DMF, room temperature, 6 d;
DOI:10.1039/P19930002657