22927-13-5

Basic information

• Product Name: 2-ETHYLBENZALDEHYDE
• Synonyms: 2-ethyl-benzaldehyd;Benzaldehyde, 2-ethyl-;6-Ethyl benzaldehyde;o-Ethylbenzaldehyde
• CAS NO: 22927-13-5
• Molecular Formula: C₉H₁₀O
• Molecular Weight: 134.18
• Product Categories: Benzaldehyde;Aldehydes;C9;Carbonyl Compounds;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 22927-13-5.mol
• Article Data: 30

Chemical Properties

• Melting Point: 210 °C
• Boiling Point: 212 °C(lit.)
• Flash Point: 230 °F
• Appearance: /
• Density: 1.02 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.2mmHg at 25°C
• Refractive Index: n20/D 1.538(lit.)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-ETHYLBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ETHYLBENZALDEHYDE(22927-13-5)
• EPA Substance Registry System: 2-ETHYLBENZALDEHYDE(22927-13-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 22927-13-5(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 22927-13-5 differently. You can refer to the following data:
1. A volatile derivative of benzaldehyde present in animal-derived food products.
2. Reactant for:Preparation of potential antibacterial agentsAsymmetric addition reactionsSolid-phase synthesis of BODIPY dyes and development of an Ig fluorescent sensorCondensation reactions with phenylenediamine or aminothiophenol catalyzed by Mesoporous mixed metal oxide nanocrystals preparaed from aero gel process

InChI:InChI=1/C9H10O/c1-2-8-5-3-4-6-9(8)7-10/h3-7H,2H2,1H3

Upstream product

• 28272-96-0 2-vinylbenzaldehyde 
• 767-90-8 (2-ethylphenyl)methanol 
• 75-17-2 formaldoxime 
• 578-54-1 ortho-ethylaniline 
• 17634-51-4 7-ethyl-1,3,5-cycloheptatriene 
• 119391-23-0 C₁₆H₁₇N₂O₃S^(1-)*Na⁽¹⁺⁾ 
• 611-14-3 2-Ethyltoluene 
• 612-19-1 2-ethylbenzoic acid 
• 493-05-0 isochromane 
• 21450-63-5 2-ethylphenylmagnesium bromide 
• 68-12-2 N,N-dimethyl-formamide 
• 97-94-9 triethyl borane 
• 84761-77-3 2-formylphenyl triflate 
• 496-11-7 INDANE 

Downstream Products

• 862074-51-9 1-(2,2-dibromovinyl)-2-ethylbenzene 
• 1027375-60-5 2-[1-(2-Ethyl-phenyl)-meth-(Z)-ylidene]-4,6-bis-(2-methoxy-ethoxymethoxy)-benzofuran-3-one 
• 103988-23-4 3-(2-ethyl-phenyl)-acrylic acid 
• 1118766-45-2 carbonyl[2-(ethylphenyl)-C]tris(trimethylphosphine)cobalt(I) 
• 1258002-49-1 (E)-2-(2-ethylbenzylidene)hydrazinecarbothioamide 
• 1250112-17-4 C₁₃H₂₁N 
• 1333161-07-1 C₁₃H₁₉N 
• 854664-97-4 3-(2-ethylphenyl)propan-1-ol 
• 129075-84-9 3-(2-ethylphenyl)propanoic acid 

Relevant articles and documents

Chromium(VI) supported and entrapped on silica and zirconia as recyclable materials for oxidation of alcohols

Oxidation of alcohols have been realized with Cr(VI) oxide supported or entrapped, via sol-gel methodology, on silica and zirconia. These materials were easily recovered from the reaction mixture without leaching of chromium in solution. Moreover, recycling studies have indicated that they can be regenerated by calcinations at 400-600°C or by treatment with ozone at room temperature. In the case of Cr(VI) entrapped into silica matrix up to 18 oxidation cycles have been realized without loss in activity.

Radical induced disproportionation of alcohols assisted by iodide under acidic conditions

The disproportionation of alcohols without an additional reductant and oxidant to simultaneously form alkanes and aldehydes/ketones represents an atom-economical transformation. However, only limited methodologies have been reported, and they suffer from a narrow substrate scope or harsh reaction conditions. Herein, we report that alcohol disproportionation can proceed with high efficiency catalyzed by iodide under acidic conditions. This method exhibits high functional group tolerance including aryl alcohol derivatives with both electron-withdrawing and electron-donating groups, furan ring alcohol derivatives, allyl alcohol derivatives, and dihydric alcohols. Under the optimized reaction conditions, a 49% yield of 5-methyl furfural and a 49% yield of 2,5-diformylfuran were obtained simultaneously from 5-hydroxymethylfurfural. An initial mechanistic study suggested that the hydrogen transfer during this redox disproportionation occurred through the inter-transformation of HI and I2. Radical intermediates were involved during this reaction.

NOVEL 6,7-DIHYDRO-4H-PYRAZOLO[1,5-A]PYRAZINE INDOLE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV)

The present invention relates generally to novel antiviral agents. Specifically, the present invention relates to compounds which can inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV replication cycle, compositions comprising such compounds, methods for inhibiting HBV viral replication, methods for treating or preventing HBV infection, and processes and intermediates for mating the compounds.

NOVEL INDOLE-2-CARBOXAMIDES ACTIVE AGAINST THE HEPATITIS B VIRUS (HBV)

The present invention relates generally to novel antiviral agents. Specifically, the present invention relates to compounds which can inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV replication cycle, compositions comprising such compounds, methods for inhibiting HBV viral replication, methods for treating or preventing HBV infection, and processes and intermediates for making the compounds.