236390-57-1

Basic information

• Product Name: 4-methoxy-2-[(prop-2-yn-1-yl)oxy]benzaldehyde
• Synonyms: 4-methoxy-2-[(prop-2-yn-1-yl)oxy]benzaldehyde
• CAS NO: 236390-57-1
• Molecular Weight: 190.199
• Mol File: 236390-57-1.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 4-methoxy-2-[(prop-2-yn-1-yl)oxy]benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-2-[(prop-2-yn-1-yl)oxy]benzaldehyde(236390-57-1)
• EPA Substance Registry System: 4-methoxy-2-[(prop-2-yn-1-yl)oxy]benzaldehyde(236390-57-1)

Safety Data

• Hazardous Substances Data: 236390-57-1(Hazardous Substances Data)

Upstream product

• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 106-96-7 propargyl bromide 

Downstream Products

• 1448162-76-2 (Z)-N-(6-methoxy-3-(phenoxymethyl)-2H-chromen-2-ylidene)-4-methylbenzenesulfonamide 

Relevant articles and documents

Microwave-Assisted Organocatalytic Intramolecular Knoevenagel/Hetero Diels-Alder Reaction with O-(Arylpropynyloxy)-Salicylaldehydes: Synthesis of Polycyclic Embelin Derivatives

A highly efficient and regioselective approach to new polycyclic embelin derivatives through a domino Knoevenagel condensation/intramolecular hetero Diels-Alder reaction using O-(arylpropynyloxy)-salicylaldehydes in the presence of ethylenediamine diacetate (EDDA) is reported. This organocatalyzed protocol is compatible toward a wide range of aryl-substituted alkynyl ethers with electron-donating and electron-withdrawing groups. When other active methylene compounds were subjected to this domino reaction the corresponding adducts were obtained in high yield.

Multicomponent and 1,3-dipolar cycloaddition synthesis of triazole- and isoxazole-acridinedione/xanthenedione heterocyclic hybrids: Cytotoxic effects on human cancer cells

A new series of diverse 1,2,3-triazole-acridinedione/xanthenedione and 1,2-isoxazole-acridinedione/xanthenedione heterocyclic hybrids have been synthesized via 1,3-dipolar coupling reaction of N/O-substituted-acridinedione-alkyne or O-substituted-xanthene

Synthesis and biological properties of novel 1-methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene) hydrazine analogues

1-Methyl-2-(2-(prop-2-yn-1-yloxy)benzylidene)hydrazine analogues were readily prepared in good yields by the reaction of 2-(prop-2-yn-1-yloxy)benzaldehydes and methyl hydrazine. The reaction tolerates a variety of substituents on the 2-hydroxybenzaldehyde