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(5H-dibenzo[d,f][1,3]diazepin-6-yl)-phenyl-methanone is a complex organic compound with the chemical formula C21H16N2O. It is a derivative of dibenzodiazepine, a class of compounds known for their potential therapeutic applications, particularly in the development of drugs for treating various central nervous system disorders. This specific compound features a dibenzodiazepine core with a phenyl group attached to a methanone (ketone) functional group. The structure is characterized by its potential to interact with biological targets, such as receptors or enzymes, which may be relevant in the context of pharmaceutical research. The compound's properties, such as solubility, stability, and reactivity, can be influenced by the presence of the phenyl and methanone moieties, making it a subject of interest for chemists and pharmacologists alike.

4511-76-6

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4511-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4511-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4511-76:
(6*4)+(5*5)+(4*1)+(3*1)+(2*7)+(1*6)=76
76 % 10 = 6
So 4511-76-6 is a valid CAS Registry Number.

4511-76-6Downstream Products

4511-76-6Relevant academic research and scientific papers

Sulfur-mediated synthesis of unsymmetrically substituted: N -aryl oxalamides by the cascade thioamidation/cyclocondensation and hydrolysis reaction

Ilment, Nikita V.,Lyssenko, Konstantin A.,Tikhonova, Tatyana A.,Volkova, Yulia A.,Zavarzin, Igor V.

, p. 5050 - 5060 (2020)

A facile and straightforward synthesis of unsymmetrically substituted N-aryl oxalamides from 2,2′-biphenyldiamines, 2-chloroacetic acid derivatives, elemental sulfur, and water has been developed. This protocol is distinguished by efficiency in water under metal-free conditions for N-aryl oxalamides bearing a side-chain NH2-group; it can be adapted for scale-up synthesis. The scope and limitations of this transformation have been investigated.

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