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3'-Methylazobenzene-4-amine is an organic compound with the chemical formula C13H14N4. It is a derivative of azobenzene, featuring a methyl group attached to the 3' position of the molecule. 3'-Methylazobenzene-4-amine is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes, which are widely used in the textile, plastics, and printing industries. Due to its chemical structure, 3'-Methylazobenzene-4-amine may exhibit certain properties such as reactivity with other chemicals and potential health or environmental concerns, which should be considered in its handling and use.

722-23-6

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722-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 722-23-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 722-23:
(5*7)+(4*2)+(3*2)+(2*2)+(1*3)=56
56 % 10 = 6
So 722-23-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H13N3/c1-10-3-2-4-13(9-10)16-15-12-7-5-11(14)6-8-12/h2-9H,14H2,1H3/b16-15+

722-23-6Relevant academic research and scientific papers

A novel procedure to synthesize 3-chloro-1-(4a,10b-diazaphenanthrene-2-yl)- 4-phenyl azetidin-2-ones and exploration of their anti-inflammatory activity

Sharma, Manisha,Maheshwari, Arti,Bindal, Nitin

, p. E116-E120 (2013/06/04)

Some new derivatives of 3-chloro-1-(4a,10b-diazaphenanthrene-2-yl)-4-phenyl azetidin-2-one were synthesized through the reaction of N-{4-[phenyldiazenyl] phenyl}-N-[phenyl methylene] amine with 4-[phenyldiazenyl] aniline. The resulting 3-chloro-4-phenyl-1-{4-[phenyldiazenyl] phenyl} azetidin-2-one intermediate in benzene was irradiated in a Pyrex vessel with 350 nm UV light in a photochemical reactor to give the desired derivatives (4a-j). Structures of the new compounds were verified on the basis of spectral and elemental methods of analyses. Nine of the prepared compounds were tested for their anti-inflammatory effects; most of these compounds showed potent and significant results compared with indomethacin.

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