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25022-59-7

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25022-59-7 Usage

General Description

The chemical compound (2-benzylaziridin-1-yl)(4-nitrophenyl)methanone is a synthetic organic molecule that consists of a benzylaziridine ring and a 4-nitrophenyl group attached to a methanone moiety. As a member of the aziridine class of compounds, it exhibits high reactivity due to the strained three-membered ring structure. The presence of the nitro group adds to its potential for biological and chemical usage, as nitro compounds are known to have a wide range of applications in various fields including pharmaceuticals, agrochemicals, and materials science. The combination of these structural features suggests that this compound may have value as a building block in the development of new drugs, agrochemicals, or materials. Additionally, it may exhibit unique reactivity and behavior that could make it useful as a catalyst or reagent in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 25022-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,2 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25022-59:
(7*2)+(6*5)+(5*0)+(4*2)+(3*2)+(2*5)+(1*9)=77
77 % 10 = 7
So 25022-59-7 is a valid CAS Registry Number.

25022-59-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-benzylaziridin-1-yl)-(4-nitrophenyl)methanone

1.2 Other means of identification

Product number -
Other names N-<p-Nitrobenzoyl>-2-benzyl-aziridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25022-59-7 SDS

25022-59-7Relevant articles and documents

RuV-Acylimido Intermediate in [RuIV(Por)Cl2]-Catalyzed C–N Bond Formation: Spectroscopic Characterization, Reactivity, and Catalytic Reactions

Che, Chi-Ming,Hong, Dan-Yan,Huang, Jie-Sheng,Law, Siu-Man,Liu, Yungen,Lo, Vanessa Kar-Yan,Toy, Patrick H.,Wu, Liangliang

supporting information, p. 18619 - 18629 (2021/06/09)

Metal-catalyzed C?N bond formation reactions via acylnitrene transfer have recently attracted much attention, but direct detection of the proposed acylnitrenoid/acylimido M(NCOR) (R=aryl or alkyl) species in these reactions poses a formidable challenge. H

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