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2-(2-Bromoethyl)benzoimidazole is a chemical compound that belongs to the benzimidazole family. It is characterized by a benzene ring fused to an imidazole ring, with a 2-bromoethyl group attached to the benzene ring. This white to off-white solid substance is soluble in organic solvents and has been the subject of various research studies due to its potential pharmaceutical applications and use as a building block for the synthesis of other compounds. Its synthesis can be achieved through different chemical reactions, and it should be handled with proper precautions in accordance with established safety guidelines.

4078-54-0

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4078-54-0 Usage

Uses

Used in Pharmaceutical Research:
2-(2-Bromoethyl)benzoimidazole is used as a pharmaceutical candidate for its potential applications in the development of new drugs. Its unique chemical structure allows it to interact with various biological targets, making it a valuable compound for exploring novel therapeutic agents.
Used in Chemical Synthesis:
As a building block, 2-(2-Bromoethyl)benzoimidazole is used in the synthesis of other compounds, particularly in the field of organic chemistry. Its presence in the final products can contribute to the desired properties and functions of the synthesized compounds, such as improved stability, reactivity, or selectivity.
Used in Research Studies:
2-(2-Bromoethyl)benzoimidazole is utilized in various research studies to investigate its properties, reactivity, and potential applications. These studies can provide valuable insights into the compound's behavior and help in the development of new methodologies and applications in different fields.
Used in Material Science:
In the field of material science, 2-(2-Bromoethyl)benzoimidazole can be used as a component in the development of new materials with specific properties. Its incorporation into polymers, coatings, or other materials can enhance their performance, such as improving their thermal stability, chemical resistance, or biocompatibility.
Used in Analytical Chemistry:
2-(2-Bromoethyl)benzoimidazole can be employed as a reagent or a reference compound in analytical chemistry. Its unique chemical structure and properties can be utilized for the development of new analytical methods, such as chromatography, spectroscopy, or electrochemistry, to detect and quantify various compounds in complex samples.

Check Digit Verification of cas no

The CAS Registry Mumber 4078-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4078-54:
(6*4)+(5*0)+(4*7)+(3*8)+(2*5)+(1*4)=90
90 % 10 = 0
So 4078-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrN2/c10-6-5-9-11-7-3-1-2-4-8(7)12-9/h1-4H,5-6H2,(H,11,12)

4078-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Bromoethyl)-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-(2-bromo-ethyl)-1H-benzoimidazole

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:4078-54-0 SDS

4078-54-0Downstream Products

4078-54-0Relevant academic research and scientific papers

Discovery of novel heteroarylmethylcarbamodithioates as potent anticancer agents: Synthesis, structure-activity relationship analysis and biological evaluation

Li, Ying-Bo,Yan, Xu,Li, Ri-Dong,Liu, Peng,Sun, Shao-Qian,Wang, Xin,Cui, Jing-Rong,Zhou, De-Min,Ge, Ze-Mei,Li, Run-Tao

, p. 217 - 230 (2016/05/02)

A series of new analogs based on the structure of lead compound 10 were designed, synthesized and evaluated for their in vitro anti-cancer activities against four selected human cancer cell lines (HL-60, Bel-7402, SK-BR-3 and MDA-MB-468). Several synthesized compounds exhibited improved anti-cancer activities comparing with lead compound 10. Among them, 1,3,4-oxadiazole analogs 17o showed highest bioactivity with IC50 values of 1.23, 0.58 and 4.29 μM against Bel-7402, SK-BR-3 and MDA-MB-468 cells, respectively. It is noteworthy that 17o has potent anti-proliferation activity toward a panel of cancer cells with relatively less cytotoxicity to nonmalignant cells. The further mechanistic study showed that it induced apoptosis and cell cycle arrest through disrupting spindle assembly in mitotic progression, indicating these synthesized dithiocarbamates represented a novel series of anti-cancer compounds targeting mitosis.

Pyridine methylamino dithio formic acid heteroaryl naphthenic base ester compound and preparation method and application thereof

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Paragraph 0097; 0098; 0099, (2017/01/02)

The invention relates to a compound as shown in a general formula (I) or pharmaceutically acceptable salts or solvates thereof, and relates to a preparation method of the compound and application thereof in preparing anti-tumor drugs. Please see the general formula (I) in the description.

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