15351-42-5 Usage
Description
Dibenzo[b,f][1,5]diazocine-6,12(5H,11H)-dione, also known as benzo[d]diazocine-6,12-dione, is a chemical compound characterized by its unique heterocyclic structure. It is a member of the diazocine class, featuring two benzene rings fused to a diazocine ring along with a dione functional group. Dibenzo[b,f][1,5]diazocine-6,12(5H,11H)-dione holds promise in pharmaceutical research and drug development due to its distinctive structural features and potential pharmacological activities, although further investigation is required to elucidate its specific properties and applications.
Uses
Used in Pharmaceutical Research:
Dibenzo[b,f][1,5]diazocine-6,12(5H,11H)-dione is utilized as a research compound for exploring its potential pharmacological activities and applications in drug development. Its unique structure may offer novel therapeutic opportunities, although more studies are needed to confirm its efficacy and safety.
Used in Drug Development:
In the field of drug development, Dibenzo[b,f][1,5]diazocine-6,12(5H,11H)-dione serves as a lead compound. It may be further modified or used as a template to design new drugs with improved pharmacological profiles. Dibenzo[b,f][1,5]diazocine-6,12(5H,11H)-dione's potential applications in medicine could be vast, depending on the outcomes of ongoing research into its properties and interactions with biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 15351-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,5 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15351-42:
(7*1)+(6*5)+(5*3)+(4*5)+(3*1)+(2*4)+(1*2)=85
85 % 10 = 5
So 15351-42-5 is a valid CAS Registry Number.
15351-42-5Relevant articles and documents
A metal-A nd base-free domino protocol for the synthesis of 1,3-benzoselenazines, 1,3-benzothiazines and related scaffolds
Putta, V. P. Rama Kishore,Gujjarappa, Raghuram,Tyagi, Ujjawal,Pujar, Prasad P.,Malakar, Chandi C.
supporting information, p. 2516 - 2528 (2019/03/07)
Efficient protocols have been described for the synthesis of 1,3-benzoselenazines, 1,3-benzothiazines, 2-aryl thiazin-4-ones and diaryl[b,f][1,5]diazocine-6,12(5H,11H)-diones. These transformations were successfully driven towards the product formation under mild acid catalyzed reaction conditions at room temperature using 2-amino aryl/hetero-aryl alkyl alcohols and amides as substrates. The merits of the present methods also rely on the easy access of rarely explored bioactive scaffolds like 1,3-benzoselenazine derivatives, for which well-documented methods are rarely known in the literature. A broad range of substrates with both electron-rich and electron-deficient groups were well-tolerated under the developed conditions to furnish the desired products in yields up to 98%. The scope of the devised method is not only restricted to the synthesis of 1,3-benzoselenazines, but it was also further extended towards the synthesis of 1,3-benzothiazines, 1,3-benzothiazinones and the corresponding eight membered N-heterocycles such as diaryl[b,f][1,5]diazocine-6,12(5H,11H)-diones.
On the reaction of anthranilic acid with thionyl chloride: Iminoketene intermediate formation
Jacob, Dominic E.,Mathew, Lopez
, p. 664 - 668 (2008/09/18)
2-(Sulfinylamino) benzoyl chloride is formed on treating anthranilic acid with thionyl chloride. The formation of iminoketene intermediate from 2-(sulfinylamino) benzoyl chloride is established and the reactions carried out using the intermediate are described.
