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3-Chloro-4-aminoazobenzene is an organic compound with the chemical formula C12H10ClN3. It is a derivative of azobenzene, featuring a chlorine atom at the 3rd position and an amino group at the 4th position on the benzene ring. This yellow crystalline solid is primarily used as an intermediate in the synthesis of various dyes and pigments, particularly in the production of azo dyes. Due to its potential health risks and environmental concerns, its use is regulated in many countries. It is important to handle 3-chloro-4-aminoazobenzene with care, as it may be harmful if inhaled, ingested, or absorbed through the skin.

722-24-7

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722-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 722-24-7 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 722-24:
(5*7)+(4*2)+(3*2)+(2*2)+(1*4)=57
57 % 10 = 7
So 722-24-7 is a valid CAS Registry Number.

722-24-7Relevant 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.

Chromium complex compound

-

, (2008/06/13)

A chromium complex compound represented as the free acid form by the formula (I): STR1 wherein X1 represents a hydrogen atom, a methyl group, a methoxy group or a sulfonic acid group; X2, X3 and X4 represent independently a hydrogen atom, a chlorine atom, a methyl gorup, a methoxy group, a carboxyl group or a sulfonic acid group; Y represents a hydrogen atom or a sulfonic acid group; Z represents a chlorine atom, a fluorine atom or --N30 (R)3 (R represents a C1 to C4 -alkyl group), STR2 and M represents a hydrogen atom or an alkali metal, a process for producing the chromium complex compound (I) and a method for dyeing cellulosic fibers with the same. The chromium complex compound represented by formula (I) is excellent in affinity to cellulosic fibers and in color-yield, build-up properties and fastness properties. These compounds are dyes for cellulosic fibers.

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