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1,3-Benzenediol, 5-[(1E)-2-(4-pyridinyl)ethenyl]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

744209-00-5

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744209-00-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is the widely recognized name for the compound, which is derived from its structure and the parent compound, pyrogallol.

Explanation

The CAS (Chemical Abstracts Service) number is a unique identifier assigned to a specific chemical compound, used for easy identification and search purposes.

Explanation

The compound's structure consists of two aromatic rings, a benzene ring and a pyridine ring, which contribute to its chemical properties and reactivity.
5. Derivative of Pyrogallol

Explanation

The compound is derived from pyrogallol, which is a trihydroxybenzene molecule. This means that it shares some properties and characteristics with pyrogallol.

Explanation

The compound is utilized in research and development for its ability to act as a reagent (a substance used to initiate a chemical reaction) and as an intermediate (a substance formed during a chemical reaction, which can be further reacted to produce the final product).

Explanation

Due to its unique structure and properties, the compound plays a role in the synthesis of a wide range of organic compounds and pharmaceuticals, making it valuable in the field of chemistry.

Explanation

The compound's unique chemical properties and structure may lead to potential applications in the fields of medicine and technology, although specific uses have not been detailed in the provided material.

Explanation

The compound's chemical properties are influenced by its structure, which includes a benzene ring and a pyridine ring, making it distinct from other compounds and potentially useful in various applications.

Structure

Contains a benzene ring and a pyridine ring

Research and Development

Used as a reagent and intermediate

Synthesis

Involved in the synthesis of various organic compounds and pharmaceuticals

Potential Applications

Medicine and technology

Chemical Properties

Unique due to its structure

Check Digit Verification of cas no

The CAS Registry Mumber 744209-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,2,0 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 744209-00:
(8*7)+(7*4)+(6*4)+(5*2)+(4*0)+(3*9)+(2*0)+(1*0)=145
145 % 10 = 5
So 744209-00-5 is a valid CAS Registry Number.

744209-00-5Relevant academic research and scientific papers

Design, synthesis, and evaluation of resveratrol derivatives as Ass1-42 aggregation inhibitors, antioxidants, and neuroprotective agents

Lu, Chuanjun,Guo, Yueyan,Li, Jianheng,Yao, Meicun,Liao, Qiongfeng,Xie, Zhiyong,Li, Xingshu

, p. 7683 - 7687 (2013/02/21)

A series of novel resveratrol derivatives were designed, synthesised and evaluated as potential therapeutic agents for the treatment of Alzheimer's disease. Among these compounds, compound 7l, (E)-5-(4-(isopropylamino)styryl) benzene-1,3-diol, exhibited potent ss-amyloid aggregation inhibition activity, which was confirmed by a ThT fluorescence assay (71.65% at 20 μM) and transmission electron microscopy (TEM). Compound 7l also exhibited good antioxidant activity (4.12 Trolox equivalents in an oxygen radical absorbance capacity assay and a 37% reduction in reactive oxygen species in cells at 10 μM). The cytotoxicity analysis of compounds 7f, 7i, 7j and 7l indicated that these compounds have lower toxicities than resveratrol at 60 μM.

Synthesis and anti-inflammatory activity of resveratrol analogs

Chen, Guoliang,Shan, Wei,Wu, Yingliang,Ren, Lixiang,Dong, Jinhua,Ji, Zhizhong

, p. 1587 - 1590 (2007/10/03)

Seventeen novel resveratrol derivatives were synthesized. Their anti-inflammatory activities were tested on xylene-induced mouse ear edema. The pharmacological results showed that some compounds have potent anti-inflammatory activities.

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