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Methyl salicylidene-2-phenylethylamine is a chemical compound with the molecular formula C16H17NO. It is an organic molecule that features a salicylidene group (a derivative of salicylaldehyde) connected to a 2-phenylethylamine moiety through a methylene bridge. methyl salicylidene-2-phenylethylamine is known for its potential applications in the synthesis of various pharmaceuticals and as a precursor in the production of certain drugs. It is also recognized for its role in the formation of certain psychoactive substances. Due to its complex structure and potential uses, methyl salicylidene-2-phenylethylamine is a subject of interest in the fields of organic chemistry and medicinal chemistry.

5879-65-2

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5879-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5879-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5879-65:
(6*5)+(5*8)+(4*7)+(3*9)+(2*6)+(1*5)=142
142 % 10 = 2
So 5879-65-2 is a valid CAS Registry Number.

5879-65-2Downstream Products

5879-65-2Relevant academic research and scientific papers

Synthesis, structure and catalytic activity of bis(phenoxyiminato)iron(III) complexes in coupling reaction of CO2 and epoxides

Al-Qaisi, Feda'a,Genjang, Nevil,Nieger, Martin,Repo, Timo

, p. 81 - 85 (2016)

Here we described the synthesis and characterization of a series of new bis(phenoxyiminato)Fe(III)-chloro complexes using a variety of techniques, including: elemental analysis, IR-, MS(EI), UV-Vis-spectroscopy, and X-ray diffraction. A solid-state structure of bis(N-salicylidene-3-phenylpropylamine)iron(III)chloride reveals a distorted square-pyramid coordination with crystallographic C2-symmetry wherein chloride occupies the axial position. Isolated complexes were also evaluated as catalysts for a coupling reaction of CO2 and various epoxides, including propylene, 1-hexene, cyclohexene and styrene oxides to form corresponding cyclic carbonates. Accordingly, the ligand structure and the solvent used influenced the catalytic activity and marked enhancement in the activity was observed using DMF as a solvent. Under optimized reaction conditions (145 °C and 10 bar of CO2) bis(N-salicylidene-2-phenylethylamine)iron(III)chloride gave cyclopropylene carbonate with considerable high TON value (1029) within 3 h.

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