474759-76-7

Basic information

• Product Name: 2-(4-TRIFLUOROMETHOXYBENZYLIDENE)-MALONONITRILE
• Synonyms: 4-(TRIFLUOROMETHOXY)BENZYLEDENEMALONITRILE;4-(TRIFLUOROMETHOXY)BENZALMALONONITRILE;2-(TRIFLUOROMETHOXY)BENZALMALONITRILE;2-(4-TRIFLUOROMETHOXYBENZYLIDENE)-MALONONITRILE;RARECHEM AL BX 0284
• CAS NO: 474759-76-7
• Molecular Formula: C₁₁H₅F₃N₂O
• Molecular Weight: 238.17
• Mol File: 474759-76-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-TRIFLUOROMETHOXYBENZYLIDENE)-MALONONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-TRIFLUOROMETHOXYBENZYLIDENE)-MALONONITRILE(474759-76-7)
• EPA Substance Registry System: 2-(4-TRIFLUOROMETHOXYBENZYLIDENE)-MALONONITRILE(474759-76-7)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 474759-76-7(Hazardous Substances Data)

Usage

General Description

2-(4-Trifluoromethoxybenzylidene)-malononitrile is a chemical compound with the molecular formula C11H5F3N2O. It is a yellow solid with a molecular weight of 242.17 g/mol and a melting point of 152-155°C. 2-(4-TRIFLUOROMETHOXYBENZYLIDENE)-MALONONITRILE is widely used in organic synthesis and pharmaceutical research due to its reactivity and potential for the development of new drugs and materials. Its unique structure and properties make it an important building block for the development of novel molecules with potential applications in various fields.

Upstream product

• 659-28-9 p-trifluoromethoxybenzaldehyde 
• 109-77-3 malononitrile 

Downstream Products

• 1204653-96-2 C₂₁H₁₆ClF₃N₆O₃ 
• 1019063-20-7 C₂₁H₁₁F₃N₂O₄ 
• 1227682-17-8 C₂₆H₁₈ClF₃N₆O₄ 
• 791619-90-4 2-amino-4-(4-trifluoromethoxyphenyl)-6-mercaptopyridine-3,5-dicarbonitrile 
• 791619-82-4 2-amino-4-(4-trifluoromethoxyphenyl)-6-phenylsulfanylpyridine-3,5-dicarbonitrile 

Relevant articles and documents

Structural simplification of bioactive natural products with multicomponent synthesis. 4. 4H-Pyrano-[2,3-b]naphthoquinones with anticancer activity

4H-Pyrano-[2,3-b]naphthoquinone is a structural motif commonly found in natural products manifesting anticancer activities. As part of a program aimed at structural simplification of bioactive natural products utilizing multicomponent synthetic processes,

Designing tetrahydroimidazo[1,2- a ]pyridine derivatives via catalyst-free Aza-Diels-Alder Reaction (ADAR) and their insecticidal evaluation

A series of tetrahydroimidazo[1,2-a]pyridine derivatives were synthesized by the reaction of 2-vinyl-4,5-dihydroimidazole derivatives with substituted benzylidenemalononitrile via a catalyst-free aza-Diels-Alder reaction. Insecticidal activities of target