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(4-Methoxy-phenyl)-(4-morpholin-4-yl-phenyl)-diazene is a complex organic compound characterized by its diazenyl functional group, which consists of two nitrogen atoms bonded together with a single bond. This molecule features a 4-methoxy-phenyl group, which is a phenyl ring (a six-carbon aromatic ring) with a methoxy substituent attached at the 4-position. Additionally, it has a 4-morpholin-4-yl-phenyl group, which is another phenyl ring with a morpholin-4-yl substituent at the 4-position. The morpholin-4-yl group is a heterocyclic structure derived from morpholine, a cyclic amine. The combination of these functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

87437-36-3

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87437-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87437-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,3 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87437-36:
(7*8)+(6*7)+(5*4)+(4*3)+(3*7)+(2*3)+(1*6)=163
163 % 10 = 3
So 87437-36-3 is a valid CAS Registry Number.

87437-36-3Downstream Products

87437-36-3Relevant academic research and scientific papers

THE EFFECTS OF CYCLIC TERMINAL GROUPS IN 4-AMINOAZOBENZENE AND RELATED AZO DYES. PART 3. ELECTRONIC ABSORPTION SPECTRA OF SOME MONOAZO DYES DERIVED FROM N-PHENYLMORPHOLINE, N-(PHENYL)THIOMORPHOLINE, N-(PHENYL)THIOMORPHOLINE 1,2-DIOXIDE, AND N-ACETYL-N'-PHENYLPIPERAZINE

Hallas, Geoffrey,Marsden, Richard,Hepworth, John D.,Mason, Donald

, p. 123 - 126 (1986)

Monoazo dyes containing a terminal morpholino group absorp hypsochromically in comparison with their piperidino counterparts as a result of electron withdrawal by the oxygen atom.Similar shifts are observed with related dyes possessing other γ-heteroatoms in the donor group.In acid solution, protonation takes place at the β-azo nitrogen atom (azonium tautomer) and at the terminal nitrogen atom (ammonium tautomer) to an extent which depends on the inductive effect of the γ-substituent.

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