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5-Bromo-1-cyclohexyl-1H-benzo[d]imidazole is a chemical compound that belongs to the benzimidazole group, which are organic compounds featuring a benzene ring fused to an imidazole ring. It is characterized by its IUPAC name and can be represented by its molecular formula C13H14BrN. With a molecular weight of 284.16 g/mol, this brominated derivative exhibits unique properties and a complex nature. Its chemical characteristics and reactivity are typically studied using methods such as nuclear magnetic resonance (NMR) and mass spectrometry (MS).

1199773-22-2

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1199773-22-2 Usage

Uses

Used in Research Applications:
5-Bromo-1-cyclohexyl-1H-benzo[d]imidazole is utilized as a research chemical for the investigation of its chemical properties and potential applications. Its unique structure and brominated nature make it a subject of interest in various scientific studies.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-Bromo-1-cyclohexyl-1H-benzo[d]imidazole is employed as a starting material or intermediate in the synthesis of new drug candidates. Its complex structure and potential interactions with biological targets make it a valuable compound for drug discovery and development.
Used in Chemical Synthesis:
5-Bromo-1-cyclohexyl-1H-benzo[d]imidazole is used as a reagent or building block in the synthesis of other complex organic compounds. Its versatility in chemical reactions allows for the creation of a wide range of molecules with potential applications in various fields.
Used in Material Science:
In material science, 5-Bromo-1-cyclohexyl-1H-benzo[d]imidazole is explored for its potential use in the development of new materials with unique properties. Its chemical structure and reactivity may contribute to the creation of advanced materials for various applications, such as electronics, coatings, or adhesives.
Used in Industrial Processes:
5-Bromo-1-cyclohexyl-1H-benzo[d]imidazole may be used in industrial processes as a catalyst, additive, or intermediate in the production of various chemical products. Its stability and reactivity under certain conditions make it a candidate for improving the efficiency and yield of certain industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1199773-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,9,7,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1199773-22:
(9*1)+(8*1)+(7*9)+(6*9)+(5*7)+(4*7)+(3*3)+(2*2)+(1*2)=212
212 % 10 = 2
So 1199773-22-2 is a valid CAS Registry Number.

1199773-22-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-1-cyclohexyl-1H-benzo[d]imidazole

1.2 Other means of identification

Product number -
Other names 5-bromo-1-cyclohexylbenzimidazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1199773-22-2 SDS

1199773-22-2Relevant academic research and scientific papers

Effective synthesis of benzimidazoles-imidazo[1,2-a]pyrazine conjugates: A comparative study of mono-and bis-benzimidazoles for antitumor activity

Singh, Iqubal,Luxami, Vijay,Paul, Kamaldeep

, p. 546 - 561 (2019)

A novel series of 6-substituted-8-(1-cyclohexyl-1H-benzo[d]imidazole-6-yl)imidazo[1,2-a]pyrazine and 6-substituted-8-(1-benzyl-1H-benzo[d]imidazole-6-yl)imidazo[1,2-a]pyrazine is first time synthesized and screen in vitro biological activity for 60 human cancer cell lines representing nine different cancer types. Derivatives 10 and 36 show antitumor activity for all tested cell lines, display comparable full panel mean-graph midpoint growth inhibition (MG_MID GI50) values of 2.10 and 2.23 μM, respectively. Furthermore, these derivatives show strong binding interactions with DNA and bovine serum albumin (BSA), studied through absorption, emission, and circular dichroism techniques. These spectroscopic studies reveal that imidazo[1,2-a]pyrazine-benzimidazoles 10 and 36, intercalate with ct-DNA as a leading interaction for fundamental biologically significant effects, with monobenzimidazole show better activity than bisbenzimidazole. These experiments have confirmed that the imidazo[1,2-a]pyrazine and benzimidazole moieties are efficient pharmacophores to trigger binding to DNA. These compounds have also interacted with bovine serum albumin protein that demonstrating high values of binding constant.

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