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8-methoxyphenanthro[3,4-d][1,3]dioxole is a complex organic chemical compound characterized by a phenanthrene core, which is a tricyclic aromatic hydrocarbon. The molecule features a 1,3-dioxole ring fused to the phenanthrene at positions 3 and 4, and an additional oxygen atom at position 8, which is connected to a methoxy group. This structure endows the compound with unique electronic and steric properties, making it a potential candidate for various applications in the fields of materials science, pharmaceuticals, and chemical research. The specific arrangement of atoms and functional groups in 8-methoxyphenanthro[3,4-d][1,3]dioxole can influence its reactivity, stability, and potential interactions with other molecules, which are important considerations in its practical applications.

35142-04-2

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35142-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35142-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,4 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35142-04:
(7*3)+(6*5)+(5*1)+(4*4)+(3*2)+(2*0)+(1*4)=82
82 % 10 = 2
So 35142-04-2 is a valid CAS Registry Number.

35142-04-2Downstream Products

35142-04-2Relevant academic research and scientific papers

Carbon-13 NMR Spectra of Some Phenanthrene Derivatives from Aristolochia indica and their Analogues

Achari, Basudeb,Bandyopadhyay, Soumitra,Chakravarty, Ajit K.,Pakrashi, Satyesh C.

, p. 741 - 746 (1984)

(13)C NMR spectra of compounds related to aristolochic acid and aristololactam, the constituents of Aristolochia indica, have been studied to determine the chemical shifts and coupling constants of polysubstituted phenanthrenes.Selective (1)H decoupling and long-range couplings were utilized for the assignments.Substituent-induced chemical shifts and also the effects on coupling constants could be deduced in some cases.Anion formation was found to be particularly helpful in the interpretation of the spectra of carboxylic compounds.Shift assignments of some structurally related compounds could also be made.

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