4886-29-7 Usage
Uses
Used in Pharmaceutical Synthesis:
1H-Benzimidazole,5-chloro-2-(1-methylethyl)-(9CI) is used as a building block in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of various drugs. Its presence in these compounds can influence their pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Antifungal and Antibacterial Applications:
1H-Benzimidazole,5-chloro-2-(1-methylethyl)-(9CI) is studied for its potential as an antifungal and antibacterial agent due to its ability to interact with microbial cells and disrupt their normal functions. Its chloro and isopropyl substituents may contribute to its antimicrobial activity, making it a candidate for further research and development in the field of infectious diseases.
Used in Coordination Chemistry:
1H-Benzimidazole,5-chloro-2-(1-methylethyl)-(9CI) has been investigated for its potential as a ligand in coordination chemistry. Its ability to form complexes with metal ions can lead to the development of new materials with specific properties, such as catalytic, optical, or electronic applications.
Used in Environmental Impact Studies:
The environmental impact of 1H-Benzimidazole,5-chloro-2-(1-methylethyl)-(9CI) is also a subject of interest. Understanding how 1H-Benzimidazole,5-chloro-2-(1-methylethyl)-(9CI) interacts with the environment, including its potential toxicity, biodegradability, and persistence, is crucial for assessing its suitability for various applications and ensuring its safe use.
Check Digit Verification of cas no
The CAS Registry Mumber 4886-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4886-29:
(6*4)+(5*8)+(4*8)+(3*6)+(2*2)+(1*9)=127
127 % 10 = 7
So 4886-29-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClN2/c1-6(2)10-12-8-4-3-7(11)5-9(8)13-10/h3-6H,1-2H3,(H,12,13)
4886-29-7Relevant academic research and scientific papers
Synthesis of 2-alkyl-substituted benzimidazoles by thermal decomposition of 2-azidobenzenamines in the presence of an aldehyde
Wallace, Jeffery M.,Soederberg, Bjoern C. G.,Hubbard, Jeremiah W.
, p. 3425 - 3439 (2007/10/03)
2-Substituted benzimidazoles were prepared by reaction of 2-azidoaminobenzenes with aldehydes under thermal conditions. The reaction probably proceeds via a sequential imine formation, azide decomposition forming a nitrene, and electrocyclization. Copyright Taylor & Francis Group, LLC.
NITRATION DE BENZIMIDAZOLES SUBSTITUES
Benchidmi, M.,Kihel, A. El,Essassi, E. M.,Knouzi, N.,Toupet, L.,et al.
, p. 605 - 612 (2007/10/02)
The mononitration of some 2-Alkyl-5(6)chloro-(or methyl-)benzimidazoles was carried out because the chemical literature results were ambiguous.Our work has shown that the nitro group was introduced in 6 (or 5) position.
SYNTHESIS AND PESTICIDAL ACTIVITY OF N,N'-DIACYL DERIVATIVES OF 4-CHLORO-1,2-PHENYLENDIAMINE
Molchanov, L. V.,Ayupova, A. T.,Kadyrov, Ch. Sh.,Shapkin, V. A.
, p. 196 - 198 (2007/10/02)
The acylation of 2-aminoacyl-chloroanilines with acid anhydrides has given N,N'-diacyl derivatives of 4-chloro-1,2-phenylenediamine.Their fungicidal activities have been investigated.It has been shown that in cotton plants they are converted into 2-alkyl-5-chlorobenzimidazoles.
