69211-06-9 Usage
Azo compound
Characterized by a diazo group (-N=N-) and a phenyl group
The compound has a diazo group (-N=N-) attached to a phenyl group, which is a key feature of azo compounds.
Hydrazine group
Attached to an acetamide group
The compound also contains a hydrazine group (-NH-NH2) attached to an acetamide group, giving it unique properties.
Physical appearance
Yellow to orange powder
The chemical appears as a yellow to orange powder, which may affect its handling and storage.
Primary use
Reagent in laboratory experiments
The main application of 2-[(E)-phenyldiazenyl]-2-(2-phenylhydrazinylidene)acetamide is as a reagent in various laboratory experiments.
Potential applications
Pharmaceutical research and development
Due to its structural properties and functional groups, the chemical may have potential applications in pharmaceutical research and development.
Safety precautions
Handle and use with caution
It is important to handle and use this chemical with caution, as it may pose risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 69211-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,1 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69211-06:
(7*6)+(6*9)+(5*2)+(4*1)+(3*1)+(2*0)+(1*6)=119
119 % 10 = 9
So 69211-06-9 is a valid CAS Registry Number.
69211-06-9Relevant academic research and scientific papers
Syntheses of formazans under phase-transfer conditions
Katritzky,Belyakov,Cheng,Durst
, p. 577 - 581 (2007/10/02)
Several 1,3,5-triarylformazans were synthesized (42-77%) using a new methodology. Azo-coupling of aryldiazonium salts with arylaldehyde arylhydrazones under mild basic conditions in two-phase liquid-liquid media is efficiently promoted by phase-transfer catalysts (onium salts or dicyclohexano-18-crown-6) at 5-25°C. The condensation of benzaldehyde with phenylhydrazine followed by phase-transfer catalyzed azo-coupling with phenyldiazonium chloride (one-pot procedure) gave 1,3,5-triphenylformazan in a 54% yield without isolation of the intermediate benzaldehyde phenylhydrazone. A double azo-coupling reaction of phenyldiazonium chloride with 9 different CH-active compounds afforded corresponding formazan only in the case of phenylpyruvic acid. Reaction in malonamide gave 3-carbamoyl-1,5-diphenylformazan instead of the expected 1,5-diphenylformazan.
