90395-45-2

Basic information

• Product Name: 4-(PYRIDIN-3-YL)BENZALDEHYDE
• Synonyms: 1-(4-(PYRIDIN-3-YL)PHENYL)ETHANONE
• CAS NO: 90395-45-2
• Molecular Formula: C₁₃H₁₁NO
• Molecular Weight: 197.23
• Mol File: 90395-45-2.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 346.7°C at 760 mmHg
• Flash Point: 171.4°C
• Appearance: /
• Density: 1.098g/cm³
• Vapor Pressure: 5.67E-05mmHg at 25°C
• Refractive Index: 1.57
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-(PYRIDIN-3-YL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(PYRIDIN-3-YL)BENZALDEHYDE(90395-45-2)
• EPA Substance Registry System: 4-(PYRIDIN-3-YL)BENZALDEHYDE(90395-45-2)

Safety Data

• Hazardous Substances Data: 90395-45-2(Hazardous Substances Data)

Usage

General Description

4-(pyridin-3-yl)benzaldehyde is a chemical compound with the molecular formula C12H9NO. It is a yellow crystalline solid that is soluble in organic solvents. 4-(PYRIDIN-3-YL)BENZALDEHYDE belongs to the class of aromatic aldehydes, and it contains a benzaldehyde group and a pyridine ring. It is commonly used as a building block in the synthesis of various pharmaceuticals and organic compounds. It is also used as a reagent in organic chemical reactions and as a flavoring agent in the food industry. 4-(pyridin-3-yl)benzaldehyde is known for its distinctive odor and is often used in the production of perfumes and fragrances. Overall, this compound has a wide range of applications in the chemical, pharmaceutical, and fragrance industries.

InChI:InChI=1/C13H11NO/c1-10(15)11-4-6-12(7-5-11)13-3-2-8-14-9-13/h2-9H,1H3

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Relevant articles and documents

Biaryl Cross-Coupling Enabled by Photo-Induced Electron Transfer

We report a protocol for aryl cross-coupling of electron-deficient aryl halides with electron-rich (hetero)arenes that is driven solely by violet light. This process takes advantage of formation of photo-excited state of electron-deficient aryl halides, that are reduced by electron-rich (hetero)arenes to form a pair of aryl anion and cation radicals. The resulting aryl anion radicals of aryl halides undergo mesolysis of the carbon-halogen bond to generate aryl radicals, that are coupled most likely with aryl cation radicals to afford functionalized biaryls. (Figure presented.).

PYRIDINE-SUBSTITUTED DIPHENYLPYRIMIDINES COMPOUNDS AND ORGANIC ELECTROLUMINESCENT DEVICES USING THE SAME

一種具式(I)結構之經吡啶取代之二苯基嘧啶化合物及使用該化合物之有機電激發光元件，其中，X1、A1及n係如同說明書中之定義。 The present invention provides pyridine-substituted diphenylpyrimidines compounds of formula (I) and an organic electroluminescent device using the same:wherein X1, A1and n are as defined in t

Novel Insights into the Combination of Metal- and Biocatalysis: Cascade One-Pot Synthesis of Enantiomerically Pure Biaryl Alcohols in Deep Eutectic Solvents

One of the pioneering examples of chemoenzymatic cascades in water such as the palladium-catalysed Suzuki-cross coupling followed by an enzymatic reduction has been revisited by the employment of a medium containing Deep Eutectic Solvents (DESs) for the catalytic performance. Thus, the unique properties of these neoteric solvents enabled to reach high substrate concentration for the overall process. Moreover, both isolated enzymes and whole cells exhibited excellent activities which allowed to obtain a set of chiral biaryl alcohols in good yields and very high enantiomeric excess (>99 %).