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N-[3,5-dimethyl-2-(2-methylpropanoyl)-4H-pyrazol-3-yl]-2-methyl-propanehydrazide is a complex organic compound with the molecular formula C13H22N4O2. It is a derivative of pyrazole, a heterocyclic compound with a five-membered aromatic ring containing three nitrogen atoms. The structure of N-[3,5-dimethyl-2-(2-methylpropanoyl)-4H-pyrazol-3-yl]-2-methyl-propanehydrazide features a pyrazole ring substituted with two methyl groups at the 3 and 5 positions, a 2-methylpropanoyl group at the 2 position, and a 2-methylpropanehydrazide group attached to the nitrogen atom. N-[3,5-dimethyl-2-(2-methylpropanoyl)-4H-pyrazol-3-yl]-2-methyl-propanehydrazide is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or other industries due to its unique structure and properties.

5679-75-4

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5679-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5679-75-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5679-75:
(6*5)+(5*6)+(4*7)+(3*9)+(2*7)+(1*5)=134
134 % 10 = 4
So 5679-75-4 is a valid CAS Registry Number.

5679-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[3,5-dimethyl-2-(2-methylpropanoyl)-4H-pyrazol-3-yl]-2-methylpropanehydrazide

1.2 Other means of identification

Product number -
Other names N-{[3,5-dimethyl-1-(2-methylpropanoyl)(2-pyrazolin-5-yl)]amino}-2-methylpropan amide

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:5679-75-4 SDS

5679-75-4Downstream Products

5679-75-4Relevant academic research and scientific papers

[3+2] Cross-coupling reactions of aziridines with isocyanates catalyzed by nickel(II) iodide

Munegumi, Takeshi,Azumaya, Isao,Kato, Takako,Masu, Hyuma,Saito, Shinichi

, p. 379 - 382 (2006)

Cycloaddition of aziridines with isocyanates proceeded smoothly in the presence of a nickel catalyst, and five iminooxazolidine derivatives were isolated in good yields. The best result was obtained when the reaction was carried out in the presence of NiI

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