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8-(p-Toluidino)-2-methylceramidonine is a chemical compound with the molecular formula C18H24N4O. It is a derivative of ceramidonine, a naturally occurring alkaloid found in certain plants. The compound features a ceramidonine core with a methyl group at the 2-position and a p-toluidino group at the 8-position. This specific arrangement of functional groups gives the compound unique properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's structure and properties make it an interesting subject for further study and exploration in the realm of organic chemistry.

7628-56-0

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7628-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7628-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7628-56:
(6*7)+(5*6)+(4*2)+(3*8)+(2*5)+(1*6)=120
120 % 10 = 0
So 7628-56-0 is a valid CAS Registry Number.

7628-56-0Relevant academic research and scientific papers

BASIC DYE MIXTURES FOR ARAMID FIBRES

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Page/Page column 11; 12, (2018/07/05)

The present invention is directed to dye mixtures comprising structures of formula and their production and their use for dyeing textiles and in particular for dyeing aramid fibres.

SYNTHESIS OF DIQUINOLINOANTHRACENE AND PYRIDINOANTHRAQUINOLINES

Kazankov, M. V.,Bernadskii, M. I.,Mustafina, M. Ya.

, p. 784 - 786 (2007/10/02)

New heterocyclic polycondensed systems - diquinolinoanthracene and pyridinoanthraquinoline - were synthesized by the action of polyphosphoric acid on 1,4-di(p-toluidino)anthraquinone and 6-arylaminoanthrapyridones.Dipyridonoanthraquinoline with an amino g

Action of Sodium Dithionite on Some Cationic Dyes

Ayyangar, N. R.,Khanna, I. K.

, p. 763 - 766 (2007/10/02)

Sodium dithionite (SDT) has been developed as a useful reagent to dequaternize a variety of cationic dyes.Triarylmethane dyes are converted into leuco bases; however, hemicyanines smoothly undergo dehydrochlorination.Phenothiazine and phenoxazine dyes on reduction with SDT give unstable leuco bases, which can be isolated as their N-benzoyl derivatives.The IR, PMR and mass spectral studies of the leuco bases or the dequaternized products have been found to be useful for structure elucidation of the cationic dyes.

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