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2-((7-methoxy-1,4-diphenethyl-1,2,3,4-tetrahydroquinoxalin-6-yl)methylene)malononitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1427042-46-3

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1427042-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427042-46-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,0,4 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1427042-46:
(9*1)+(8*4)+(7*2)+(6*7)+(5*0)+(4*4)+(3*2)+(2*4)+(1*6)=133
133 % 10 = 3
So 1427042-46-3 is a valid CAS Registry Number.

1427042-46-3Downstream Products

1427042-46-3Relevant academic research and scientific papers

Synthesis, photophysical properties, and antimicrobial activity of novel styryl colorants derived from 7-methoxy-1,4-diphenethyl-1,2,3,4- tetrahydroquinoxaline-6-carbaldehyde

Jarag,Jagtap,Borse,Shukla,Shankarling

, p. 1196 - 1201 (2013/01/15)

The novel 1,4-diphenethyl-1,2,3,4-tetrahydro-7-methoxyquinoxalin-6- carbaldehyde was synthesized by reductive alkylation of 6-methoxy quinoxaline with phenyl acetic acid and was further subjected to Knoevenagel condensation with various active methylene compounds to synthesize novel styryl colorants. Photophysical properties of styryl colorants were studied using UV-visible and fluorescence spectroscopy. These colorants displayed orange to violet hue and showed fluorescence emission maxima in the region of 560-640 nm, and displayed a large Stokes shift (85-104 nm). Compounds were subjected to thermogravimetric analysis which showed excellent stability up to 310°C. These styryl compounds were evaluated for their antimicrobial study as antifungal against Candida albicans C. albicans and Aspergillus niger and antibacterial against Escherichia coli and Staphylococcus aureus. The results revealed good antimicrobial activity against tested organisms. The synthesized chromophores were characterized using elemental analysis, FTIR, 13C-NMR and 1H-NMR spectroscopy and mass spectrometry.

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