Ethanone, 1-[2-[4-[3-[[2-(3,4-dimethoxyphenyl)ET

Base Information

Chemical Name:Ethanone, 1-[2-[4-[3-[[2-(3,4-dimethoxyphenyl)ET
CAS No.:102152-21-6
Molecular Formula:C₂₅H₃₁N₃O₅
Molecular Weight:453.538
Hs Code.:
ChEMBL ID:CHEMBL10813
DSSTox Substance ID:DTXSID20875530

Synonyms:CHEMBL10813;SCHEMBL10555823;DTXSID20875530;ETHANONE, 1-[2-[4-[3-[[2-(3,4-DIMETHOXYPHENYL)ET;BDBM50405444;102152-21-6

Suppliers and Price of Ethanone, 1-[2-[4-[3-[[2-(3,4-dimethoxyphenyl)ET

Supply Marketing:

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

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Chemical Property of Ethanone, 1-[2-[4-[3-[[2-(3,4-dimethoxyphenyl)ET

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:12
Exact Mass:453.22637110
Heavy Atom Count:33
Complexity:586

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(N=C(N1)C2=CC=C(C=C2)OCC(CNCCC3=CC(=C(C=C3)OC)OC)O)C(=O)C

Technology Process of Ethanone, 1-[2-[4-[3-[[2-(3,4-dimethoxyphenyl)ET

There total 5 articles about Ethanone, 1-[2-[4-[3-[[2-(3,4-dimethoxyphenyl)ET 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:

: (S)-5-[4-(4-Acetyl-5-methyl-1H-imidazol-2-yl)-phenoxymethyl]-3-[2-(3,4-dimethoxy-phenyl)-ethyl]-oxazolidin-2-one

: 102152-21-6
(S)-5-acetyl-2-<4-<3-<<2-(3,4-dimethoxyphenyl)ethyl>amino>-2-hydroxypropoxy>phenyl>-4-methylimidazole

Guidance literature:: With sodium hydroxide; In ethanol; for 2h; Yield given; Heating;
DOI:10.1021/jm00156a028

Reference yield:

: 77335-89-8
5-acetyl-2-(4-methoxyphenyl)-4-methylimidazole

: 102152-21-6
(S)-5-acetyl-2-<4-<3-<<2-(3,4-dimethoxyphenyl)ethyl>amino>-2-hydroxypropoxy>phenyl>-4-methylimidazole

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / 48percent HBr / acetic acid / 2.5 h / Heating

2: 1.) NaH / 1.) Me₂SO, 60 deg C, 15 min, 2.) Me₂SO, 60 deg C, overnight

3: 10percent NaOH / ethanol / 2 h / Heating

With sodium hydroxide; hydrogen bromide; sodium hydride; In ethanol; acetic acid;
DOI:10.1021/jm00156a028

Reference yield:

: 2393-23-9
4-methoxy-benzylamine

: 102152-21-6
(S)-5-acetyl-2-<4-<3-<<2-(3,4-dimethoxyphenyl)ethyl>amino>-2-hydroxypropoxy>phenyl>-4-methylimidazole

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) EtOAc, reflux, 2 h, 2.) CH₃CN, reflux, 19 h

2: 98 percent / 48percent HBr / acetic acid / 2.5 h / Heating

3: 1.) NaH / 1.) Me₂SO, 60 deg C, 15 min, 2.) Me₂SO, 60 deg C, overnight

4: 10percent NaOH / ethanol / 2 h / Heating

With sodium hydroxide; hydrogen bromide; sodium hydride; In ethanol; acetic acid;
DOI:10.1021/jm00156a028