24067-35-4 Usage
Uses
Used in Organic Synthesis:
N-(2-CHLORO-PHENYL)-GUANIDINE is used as a reagent in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its unique structure allows it to participate in a range of chemical reactions, facilitating the creation of diverse compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, N-(2-CHLORO-PHENYL)-GUANIDINE is utilized as a key intermediate in the synthesis of drugs. Its ability to inhibit certain enzymes makes it a valuable component in the development of medications targeting specific biological pathways.
Used in Agrochemical Production:
N-(2-CHLORO-PHENYL)-GUANIDINE also finds application in the agrochemical sector, where it serves as a precursor in the production of pesticides and other agricultural chemicals. Its role in these products is crucial for enhancing crop protection and yield.
Used as an Enzyme Inhibitor:
Due to its capacity to inhibit specific enzymes, N-(2-CHLORO-PHENYL)-GUANIDINE is employed in biological research and drug discovery. Its enzyme-inhibiting properties make it a potential candidate for the development of treatments targeting enzyme-related diseases.
Used in Biological Process Mediation:
N-(2-CHLORO-PHENYL)-GUANIDINE's role in mediating biological processes positions it as a significant compound in understanding and potentially manipulating various biological mechanisms. This application is vital for advancing knowledge in the life sciences and developing new therapeutic approaches.
Check Digit Verification of cas no
The CAS Registry Mumber 24067-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,6 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24067-35:
(7*2)+(6*4)+(5*0)+(4*6)+(3*7)+(2*3)+(1*5)=94
94 % 10 = 4
So 24067-35-4 is a valid CAS Registry Number.
24067-35-4Relevant academic research and scientific papers
Copper-promoted one-pot approach: Synthesis of benzimidazoles
Adil, Syed Farooq,Alduhaish, Osamah,Assal, Mohamed E.,Bollikolla, Hari Babu,Gollapudi, Ravi Kumar,Murthy Boddapati, S. N.,Nurbasha, Sharmila,Siddiqui, Mohammed Rafiq H.,Tamminana, Ramana
, (2020/04/24)
A facile, one-pot, and proficient method was developed for the production of various 2-arylaminobenzimidazoles. This methodology is based for the first time on a copper catalyst promoted domino C-N cross-coupling reaction for the generation of 2-arylaminobenzimidazoles. Mechanistic investigations revealed that the synthetic pathway involves a copper-based desulphurization/nucleophilic substitution and a subsequent domino intra and intermolecular C-N cross-coupling reactions. Some of the issues typically encountered during the synthesis of 2-arylaminobezimidazoles, including the use of expensive catalytic systems and the low reactivity of bromo precursors, were addressed using this newly developed copper-catalyzed method. The reaction procedure is simple, generally with excellent substrate tolerance, and provides good to high yields of the desired products.
Improved Method for the Preparation of Guanidines
Kim, Kyoung Soon,Qian, Ligang
, p. 7677 - 7680 (2007/10/02)
Use of N,N'-di-(tert-butoxycarbonyl)thiourea 1 in the presence of mercuric chloride provides a very efficient method for the bis-Boc protected guanidine formation of the amino compounds which are highly deactivated either sterically or electronically.
