1-Benzoyl-2-aziridinecarbonitrile

Base Information

Chemical Name:1-Benzoyl-2-aziridinecarbonitrile
CAS No.:1750-09-0
Molecular Formula:C₁₀H₈N₂O
Molecular Weight:172.186
Hs Code.:
DSSTox Substance ID:DTXSID901300313
Nikkaji Number:J435.742F

Synonyms:1-Benzoyl-2-aziridinecarbonitrile;DTXSID901300313;1750-09-0

Suppliers and Price of 1-Benzoyl-2-aziridinecarbonitrile

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 1-Benzoyl-2-aziridinecarbonitrile

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:172.063662883
Heavy Atom Count:13
Complexity:259

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(N1C(=O)C2=CC=CC=C2)C#N

Technology Process of 1-Benzoyl-2-aziridinecarbonitrile

There total 2 articles about 1-Benzoyl-2-aziridinecarbonitrile 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: 90.0%

: 33898-53-2
2-cyanoaziridine

: 98-88-4
benzoyl chloride

: 1750-09-0
N-Benzoylaziridin-2-carbonitril

Guidance literature:: With triethylamine; In dichloromethane; 1) 40 min, 0-5 deg C 2) 3 h, r.t.;
DOI:10.1002/hlca.19900730524

Reference yield:

: 1750-09-0
N-Benzoylaziridin-2-carbonitril

Guidance literature:: PhCONHCH2CH(CN)Cl, NH3;

Reference yield:

: 1750-09-0
N-Benzoylaziridin-2-carbonitril

: 123-54-6,81235-32-7
acetylacetone

: 138478-59-8
2-benzoylamino-5-oxohexanenitrile

: 138478-58-7
4-acetyl-2-benzoylamino-5-oxohexanenitrile

Guidance literature:: With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium hydride; Yield given. Multistep reaction. Yields of byproduct given; 1) THF, 2) THF, 4 h, reflux;