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61254-27-1

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61254-27-1 Usage

General Description

"(4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-2,5-diphenyl-2,4-dihydro-3H-pyrazol-3-one" is a compound with the chemical formula C21H21N3OS. It contains an aziridinyl group, a sulfur atom, and a pyrazolone ring. The compound is a potential anti-cancer agent, as the aziridinyl group is known to be toxic to cancer cells. The presence of the sulfur atom also suggests potential applications in organic synthesis and as a precursor for pharmaceutical compounds. Overall, "(4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-2,5-diphenyl-2,4-dihydro-3H-pyrazol-3-one" has promising properties for medicinal and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 61254-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,5 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61254-27:
(7*6)+(6*1)+(5*2)+(4*5)+(3*4)+(2*2)+(1*7)=101
101 % 10 = 1
So 61254-27-1 is a valid CAS Registry Number.

61254-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-2,5-diphenylpyrazol-3-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:61254-27-1 SDS

61254-27-1Relevant articles and documents

Reaction of Ketene Dithioacetals with Aziridine. A New Synthesis of N-Vinylaziridines and their Iodide Ion-assisted Rearrangement to Pyrrolines

Basaveswara Rao,Suresh,Kumar, Arvind,Ila,Junjappa

, p. 955 - 960 (2007/10/03)

The ketene dithioacetals 1, 4, 9 and 11 react readily with aziridine 2 to give the corresponding N-vinylaziridines 3, 5, 8 and 12 respectively, which on iodide ion-catalyzed rearrangement undergo ring expansion to give pyrrolines 14, 18, 21 and 22 respect

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