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(4-methyl-benzylidene)-thiazol-2-yl-amine is a chemical compound with the molecular formula C12H10N2S. It is a derivative of thiazol-2-yl-amine, featuring a 4-methyl-benzylidene group attached to the nitrogen atom. (4-methyl-benzylidene)-thiazol-2-yl-amine is characterized by its aromatic structure, with a methyl group attached to the benzene ring, which contributes to its stability and reactivity. It is often used in the synthesis of various pharmaceuticals and agrochemicals due to its potential to form complex molecular structures. The compound's properties, such as its solubility and reactivity, can be influenced by the presence of the methyl group and the thiazol-2-yl-amine moiety, making it a versatile building block in organic chemistry.

59775-50-7

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59775-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59775-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,7 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59775-50:
(7*5)+(6*9)+(5*7)+(4*7)+(3*5)+(2*5)+(1*0)=177
177 % 10 = 7
So 59775-50-7 is a valid CAS Registry Number.

59775-50-7Relevant academic research and scientific papers

ELECTRON IMPACT MASS SPECTRA OF para-SUBSTITUTED N-HETEROARYL BENZYLAMINES

Fioravanti, Rossella,Biava, Mariangela,Poretta, Giulio Cesare,Foti, Salvatore,Masumarra, Giuseppe,Saletti, Rosaria

, p. 367 - 378 (2007/10/02)

The 70 eV electron impact mass spectra of some para-substituted N-heteroaryl benzylamines, synthesized through the corresponding Schiff bases, are reported.Typical fragmentation patterns are discussed with the aid of mass analyzed ion kinetic energy spectra and exact mass measurements.The compounds are relatively stable under electron impact, the molecular ion being the base peak or the second most intense ion in the spectra.The dominating breakdown process is the benzylic cleavage, that gives rise to the base peak in some of the investigated compounds and to the second intense peak in others.

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