3-Benzyl-1-oxo-1lambda~5~-pyrazine

Base Information

Chemical Name:3-Benzyl-1-oxo-1lambda~5~-pyrazine
CAS No.:90210-59-6
Molecular Formula:C₁₁H₁₀N₂O
Molecular Weight:186.213
Hs Code.:
DSSTox Substance ID:DTXSID00521543
Wikidata:Q82386076

Synonyms:3-Benzyl-1-oxo-1lambda~5~-pyrazine;90210-59-6;DTXSID00521543

Suppliers and Price of 3-Benzyl-1-oxo-1lambda~5~-pyrazine

Supply Marketing:

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

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Chemical Property of 3-Benzyl-1-oxo-1lambda~5~-pyrazine

Chemical Property:

XLogP3:0.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:186.079312947
Heavy Atom Count:14
Complexity:169

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC2=NC=C[N+](=C2)[O-]

Technology Process of 3-Benzyl-1-oxo-1lambda~5~-pyrazine

There total 2 articles about 3-Benzyl-1-oxo-1lambda~5~-pyrazine 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: 40.0%

: 28217-95-0
2-benzylpyrazine

: 90210-53-0
2-benzylpyrazine N₁-oxide

: 90210-59-6
3-Benzylpyrazine 1-oxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In benzene; for 18h; Ambient temperature;
DOI:10.1055/s-1983-30619

Reference yield:

: 90210-53-0
2-benzylpyrazine N₁-oxide

: 90210-59-6
3-Benzylpyrazine 1-oxide

Guidance literature:: Multi-step reaction with 2 steps

1: 15 percent / 800 °C / 0 - 0 Torr

2: 40 percent / 70percent m-chloroperbenzoic acid / benzene / 18 h / Ambient temperature

With 3-chloro-benzenecarboperoxoic acid; In benzene;
DOI:10.1055/s-1983-30619