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"N'-(5-phenyl-[1,3,4]oxadiazol-2-yl)-benzohydrazonoyl bromide" is a complex organic chemical compound with the molecular formula C19H12BrN3O2. It features a benzohydrazonoyl group attached to a 5-phenyl-[1,3,4]oxadiazol-2-yl moiety, which is a heterocyclic ring system. N'-(5-phenyl-[1,3,4]oxadiazol-2-yl)-benzohydrazonoyl bromide is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. It is typically used in research and development settings, where its properties can be exploited to create new compounds or improve existing ones. The compound's specific applications may vary, but it is generally recognized for its role in the field of organic synthesis and medicinal chemistry.

35223-06-4

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35223-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35223-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35223-06:
(7*3)+(6*5)+(5*2)+(4*2)+(3*3)+(2*0)+(1*6)=84
84 % 10 = 4
So 35223-06-4 is a valid CAS Registry Number.

35223-06-4Relevant academic research and scientific papers

Reactions of bromine and lead tetra-acetate with 2-(substituted hydrazino)-5-phenyl-1,3,4-oxadiazoles: Routes to 3-aryl-6-phenyl-1,2,4- triazolo[3,4-b][1,3,4]oxadiazoles

Butler,Lambe,Scott

, p. 269 - 273 (2007/10/04)

2-(Substituted hydrazino)-5-phenyl-1,3,4-oxadiazoles react with bromine in acetic acid to yield hydrazone perbromides, or hydrazonyl bromides in the presence of sodium acetate. Treatment of the hydrazonyl bromides with triethylamine in benzene or solvolys

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