2-Ethyl-4-methyl-6-phenylpyrimidine

Base Information

Chemical Name:2-Ethyl-4-methyl-6-phenylpyrimidine
CAS No.:89966-70-1
Molecular Formula:C₁₃H₁₄N₂
Molecular Weight:198.268
Hs Code.:
DSSTox Substance ID:DTXSID30522503
Wikidata:Q82387827

Synonyms:2-Ethyl-4-methyl-6-phenylpyrimidine;89966-70-1;SCHEMBL10271988;DTXSID30522503

Suppliers and Price of 2-Ethyl-4-methyl-6-phenylpyrimidine

Supply Marketing:

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

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Chemical Property of 2-Ethyl-4-methyl-6-phenylpyrimidine

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:198.115698455
Heavy Atom Count:15
Complexity:187

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=NC(=CC(=N1)C2=CC=CC=C2)C

Technology Process of 2-Ethyl-4-methyl-6-phenylpyrimidine

There total 1 articles about 2-Ethyl-4-methyl-6-phenylpyrimidine 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: 66.0%

: 74-96-4
ethyl bromide

: 32785-40-3
2-chloro-4-phenyl-6-methylpyrimidine

: 89966-70-1
2-ethyl-4-methyl-6-phenylpyrimidine

Guidance literature:: With 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); magnesium; In diethyl ether; for 5h; Heating;

Reference yield: 44.0%

: 89966-70-1
2-ethyl-4-methyl-6-phenylpyrimidine

: 89966-76-7
2-ethyl-6-methyl-4-phenylpyrimidine 1-oxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid;

Reference yield:

: 89966-70-1
2-ethyl-4-methyl-6-phenylpyrimidine

: 89966-80-3
4-chloromethyl-2-ethyl-6-phenylpyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: 44 percent / m-chloroperbenzoic acid

2: 77 percent / phosphoryl chloride / dioxane / Heating

With 3-chloro-benzenecarboperoxoic acid; trichlorophosphate; In 1,4-dioxane;