S-(1-Benzoyl-3-methyl-2,3-diphenylaziridin-2-yl) ethanethioate

Base Information

Chemical Name:S-(1-Benzoyl-3-methyl-2,3-diphenylaziridin-2-yl) ethanethioate
CAS No.:89873-97-2
Molecular Formula:C₂₄H₂₁NO₂S
Molecular Weight:387.502
Hs Code.:
DSSTox Substance ID:DTXSID90532840

Synonyms:89873-97-2;S-(1-Benzoyl-3-methyl-2,3-diphenylaziridin-2-yl) ethanethioate;DTXSID90532840

Suppliers and Price of S-(1-Benzoyl-3-methyl-2,3-diphenylaziridin-2-yl) ethanethioate

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of S-(1-Benzoyl-3-methyl-2,3-diphenylaziridin-2-yl) ethanethioate

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:387.12930009
Heavy Atom Count:28
Complexity:589

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)SC1(C(N1C(=O)C2=CC=CC=C2)(C)C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of S-(1-Benzoyl-3-methyl-2,3-diphenylaziridin-2-yl) ethanethioate

There total 3 articles about S-(1-Benzoyl-3-methyl-2,3-diphenylaziridin-2-yl) ethanethioate 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:

: 98-88-4
benzoyl chloride

: 89873-97-2
2,3-Diphenyl-2-(acetylthio)-1-benzoyl-3-methylaziridine

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent

2: 2) N(C₂H₅)3 / 1.) hv, toluene, -78 deg C, 2.) -78 deg C

With triethylamine;
DOI:10.1021/jo00184a037

Reference yield:

: 64551-86-6
N-[1-phenylethyl]benzenecarbothioamide

: 89873-97-2
2,3-Diphenyl-2-(acetylthio)-1-benzoyl-3-methylaziridine

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent

2: 2) N(C₂H₅)3 / 1.) hv, toluene, -78 deg C, 2.) -78 deg C

With triethylamine;
DOI:10.1021/jo00184a037

Reference yield:

: 89873-87-0
N-(1-Phenyl-ethyl)-N-thiobenzoyl-benzamide

: 75-36-5
acetyl chloride

: 89873-93-8
N-(1-Methyl-1,2-diphenyl-2-thioxo-ethyl)-benzamide

: 89873-97-2
2,3-Diphenyl-2-(acetylthio)-1-benzoyl-3-methylaziridine

Guidance literature:: With triethylamine; Yield given. Multistep reaction. Yields of byproduct given; 1.) hv, toluene, -78 deg C, 2.) -78 deg C;
DOI:10.1021/jo00184a037