2-(2-Amino-1,3-selenazol-4-yl)-2-methyl-1-phenylpropan-1-one

Base Information

Chemical Name:2-(2-Amino-1,3-selenazol-4-yl)-2-methyl-1-phenylpropan-1-one
CAS No.:92406-01-4
Molecular Formula:C₁₃H₁₄N₂OSe
Molecular Weight:293.227
Hs Code.:
DSSTox Substance ID:DTXSID60523947
Wikidata:Q82390421

Synonyms:92406-01-4;2-(2-Amino-1,3-selenazol-4-yl)-2-methyl-1-phenylpropan-1-one;DTXSID60523947

Suppliers and Price of 2-(2-Amino-1,3-selenazol-4-yl)-2-methyl-1-phenylpropan-1-one

Supply Marketing:

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

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Chemical Property of 2-(2-Amino-1,3-selenazol-4-yl)-2-methyl-1-phenylpropan-1-one

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:294.02713
Heavy Atom Count:17
Complexity:287

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C1=C[Se]C(=N1)N)C(=O)C2=CC=CC=C2

Technology Process of 2-(2-Amino-1,3-selenazol-4-yl)-2-methyl-1-phenylpropan-1-one

There total 2 articles about 2-(2-Amino-1,3-selenazol-4-yl)-2-methyl-1-phenylpropan-1-one 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: 53.0%

: 630-10-4
selenourea

: 92406-11-6
4-Bromo-2,2-dimethyl-1-phenyl-butane-1,3-dione

: 92406-01-4
2-(2-Amino-selenazol-4-yl)-2-methyl-1-phenyl-propan-1-one

Guidance literature:: In acetonitrile; for 4h; Heating;
DOI:10.1002/jhet.5570210113

Reference yield:

: 3815-34-7
2,2-dimethyl-1-phenyl-1,3-butanedione

: 92406-01-4
2-(2-Amino-selenazol-4-yl)-2-methyl-1-phenyl-propan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / Br₂ / acetic acid / 3 h / Ambient temperature

2: 53 percent / acetonitrile / 4 h / Heating

With bromine; In acetic acid; acetonitrile;
DOI:10.1002/jhet.5570210113