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N-cinnamylidene 4-amino-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35554-48-4

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35554-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35554-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,5 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35554-48:
(7*3)+(6*5)+(5*5)+(4*5)+(3*4)+(2*4)+(1*8)=124
124 % 10 = 4
So 35554-48-4 is a valid CAS Registry Number.

35554-48-4Downstream Products

35554-48-4Relevant academic research and scientific papers

Spin crossover in polymeric materials using schiff base functionalized triazole ligands

Scott, Hayley S.,Ross, Tamsyn M.,Moubaraki, Boujemaa,Murray, Keith S.,Neville, Suzanne M.

, p. 803 - 812 (2013)

Functionalized 1,2,4-(R)-triazole-based Schiff base (RN= CH-R') ligands have been incorporated into spin crossover 1D materials of the general formula [Fe(Xtrz)3](A)2··2H2O (A = BF4, ClO4, Br, NO

USE OF DYNAMIC MIXTURES FOR A CONTROLLED RELEASE OF FRAGRANCES

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Page/Page column 34-37, (2008/06/13)

The present invention relates to a delivery system in the form of a dynamic mixture obtained by reacting together, in the presence of water, at least one hydrazine derivative with at least one perfuming, flavoring, insect repellent or attractant, bactericide and/or fungicide aldehyde or ketone. The invention's mixture is capable of releasing in a controlled and prolonged manner said aldehyde or ketone in the surrounding environment. Furthermore, the present invention concerns also the use of said dynamic mixtures as perfuming ingredients as well as the perfuming compositions or perfumed articles comprising the invention's mixtures.

A new class of antifungal agents. Synthesis and antimycotic activity of disubstituted N-azolylamines

Castellano, Sabrina,Stefancich, Giorgio,Musiu, Chiara,La Colla, Paolo

, p. 299 - 304 (2007/10/03)

In this study we extended our exploration of the N-azolylamine moiety for its antifungal activity. We prepared a number of N-azolylamino derivatives. The synthetic sequence includes the preparation of aminoazole Schiff bases, and the reduction and the alk

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