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(4-Methoxy-phenyl)-glyoxal-bis-phenylhydrazone is a complex organic compound with the molecular formula C20H20N4O2. It is derived from glyoxal, a dialdehyde, and phenylhydrazine, an aromatic hydrazine. (4-methoxy-phenyl)-glyoxal-bis-phenylhydrazone is characterized by the presence of a 4-methoxy-phenyl group attached to the glyoxal moiety, which is then reacted with two molecules of phenylhydrazine to form bis-phenylhydrazone. The resulting product is a yellow crystalline solid that is often used in chemical research and as an analytical reagent. Its structure features a central carbonyl group flanked by two phenylhydrazone groups, with the 4-methoxy-phenyl group providing additional steric and electronic effects. (4-methoxy-phenyl)-glyoxal-bis-phenylhydrazone is of interest due to its potential applications in the synthesis of various organic molecules and its use in the detection of aldehydes and ketones.

7397-16-2

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7397-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7397-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7397-16:
(6*7)+(5*3)+(4*9)+(3*7)+(2*1)+(1*6)=122
122 % 10 = 2
So 7397-16-2 is a valid CAS Registry Number.

7397-16-2Downstream Products

7397-16-2Relevant academic research and scientific papers

α,α-dibromoketones as useful precursors in organic synthesis: A simple and efficient synthesis of 2,4-diaryl- 1,2,3-triazoles via oxidative cyclization of bisphenylhydrazones

Arora, Loveena,Sharma, Nisha,Kapoor, Jitander K.

, p. 291 - 296 (2019/01/18)

α,α-Dibromoacetophenones (1a-1f) on reaction with phenylhydrazine afford corresponding arylglyoxal bisphenylhydrazones (2a-2f). The oxidation of bishydrazones 2a-2f by using copper(II) chloride in acetic acid leads to intramolecular cyclization with the formation of 2,4-diaryl-1,2,3-triazoles (3a-3f). The method for the conversion 1 → 3 has been simplified by developing one-pot procedure without isolation of intermediates 2.

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