24652-66-2

Basic information

• Product Name: Benzaldehyde, 2-fluoro-, oxime, (E)- (9CI)
• Synonyms: Benzaldehyde, 2-fluoro-, oxime, (E)- (9CI);Benzaldehyde, 2-fluoro-, oxiMe, (E)-;(E)-2-Fluorobenzaldehyde OxiMe;(E)-N-[(2-fluorophenyl)methylidene]hydroxylamine;_x005f\r(E)-2-Fluorobenzaldehyde Oxime;(NE)-N-[(2-fluorophenyl)methylidene]hydroxylamine
• CAS NO: 24652-66-2
• Molecular Formula: C₇H₆FNO
• Molecular Weight: 139.1270432
• Product Categories: OXIME
• Mol File: 24652-66-2.mol
• Article Data: 46

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Benzaldehyde, 2-fluoro-, oxime, (E)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-fluoro-, oxime, (E)- (9CI)(24652-66-2)
• EPA Substance Registry System: Benzaldehyde, 2-fluoro-, oxime, (E)- (9CI)(24652-66-2)

Safety Data

• Hazardous Substances Data: 24652-66-2(Hazardous Substances Data)

Usage

Uses

(E)-2-Fluorobenzaldehyde oxime is used as a reactant in the preparation of fluorine-19 and prediction of N-F spin-spin coupling.

Upstream product

• 446-52-6 2-Fluorobenzaldehyde 
• 462-06-6 fluorobenzene 
• 75-52-5 nitromethane 
• 5470-11-1 hydroxylamine hydrochloride 

Downstream Products

• 39502-43-7 2-fluoro-N-hydroxybenzenecarboxymidoyl chloride 
• 953046-62-3 [3-(2-fluorophenyl)isoxazol-5-yl]methanol 
• 139060-01-8 2-Fluoro-benzonitrile N-oxide 
• 1338603-96-5 C₁₂H₈F₇N₃O₅S₂ 
• 1337539-51-1 C₂₆H₃₁FN₄O 
• 1337539-57-7 C₂₆H₃₀F₂N₄O 
• 1337539-61-3 C₂₆H₃₀ClFN₄O 
• 1337539-65-7 C₂₆H₃₀ClFN₄O 
• 1337539-68-0 C₂₇H₃₃FN₄O₂ 
• 1337539-72-6 C₂₆H₃₀F₂N₄O 
• 1337539-73-7 C₃₃H₃₅F₃N₄O 
• 1337539-74-8 C₂₇H₃₃FN₄O 
• 1337539-75-9 C₂₆H₃₀ClFN₄O 
• 394-47-8 2-fluorobenzonitrile 

Relevant articles and documents

HCl-mediated cascade cyclocondensation of oxygenated arylacetic acids with arylaldehydes: one-pot synthesis of 1-arylisoquinolines

In this paper, a concise, open-vessel synthesis of 1-arylisoquinolines is describedviaHCl-mediated intermolecular cyclocondensation of oxygenated arylacetic acids with arylaldehydes in the presence of NH2OH and alcoholic solvents under mild and one-pot reaction conditions. A plausible mechanism is proposed and discussed herein. In the overall reaction process, only water was generated as the byproduct. Various environmentally friendly reaction conditions are investigated for convenient transformationviathe (4C + 1C + 1N) annulation. This protocol provides a highly effective ring closureviathe formations of one carbon-carbon (C-C) bond, two carbon-nitrogen (C-N) bonds and one carbon-oxygen (C-O) bond.

Osthole isoxazoline derivative as well as preparation method and application thereof

The invention discloses an isoxazolinyl osthole derivative, a preparation method thereof and application of the isoxazolinyl sthole derivative as an insecticide. The chemical structure of the isoxazolinyl osthole derivative is shown as a general formula (

Triazole alcohol derivative as well as preparation method and application thereof

The invention relates to a triazole alcohol derivative as well as a preparation method and application thereof. The chemical structure of the triazole alcohol derivative is shown as a formula I, R1 represents a benzene ring or a substituted benzene ring, and substituent groups of the substituted benzene ring can be located at all positions of the benzene ring, can be mono-substituted or multi-substituted, and can be selected from a) halogen which is F and Cl; b) an electron withdrawing group which is cyano or trifluoromethyl; c ) a lower alkyl of 1-4 carbon atoms or a halogen substituted loweralkyl; and d) lower alkoxy of 1-4 carbon atoms or halogen substituted lower alkoxy. The compound of the invention has strong antifungal activity, has the advantages of low toxicity, wide antibacterial spectrum and the like, and can be used for preparing antifungal drugs.