96601-10-4

Usage

Uses

Used in Plastics and Resin Industry:
2,4-bis(prop-2-yloxy)benzaldehyde is used as a chemical intermediate for the production of various polymers, which are essential in the manufacturing of plastics and resins. Its reactivity allows for the formation of stable polymers with desired properties.
Used in Coatings and Adhesives Industry:
In the coatings and adhesives industry, 2,4-bis(prop-2-en-1-yloxy)benzaldehyde is employed as a chemical intermediate to produce high-quality coatings and adhesives with enhanced bonding and durability.
Used in Organic Synthesis:
2,4-bis(prop-2-en-1-yloxy)benzaldehyde is used as a reagent in organic synthesis for the preparation of other complex organic compounds. Its reactivity enables the synthesis of a wide range of organic molecules with diverse applications.
Safety Precautions:
Due to the potential hazards and toxicity associated with 2,4-bis(prop-2-en-1-yloxy)benzaldehyde, it is crucial to follow proper safety protocols when handling this chemical. This includes wearing appropriate personal protective equipment, working in well-ventilated areas, and implementing measures to prevent accidental exposure or ingestion.

Upstream product

• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 106-95-6 allyl bromide 

Downstream Products

• 1384833-32-2 3,5-diallyl-2,4-bisallyloxybenzaldehyde 
• 1522361-73-4 (E)-1-(2,4-bis(allyloxy)-5-chlorophenyl)-3-(2,4-bis(allyloxy)phenyl)prop-2-en-1-one 
• 1522361-81-4 (E)-1-(5-chloro-2,4-dihydroxyphenyl)-3-(2,4-dihydroxyphenyl)prop-2-en-1-one 
• 1416159-06-2 (2S,3R,4S,5R,6R)-2-(4-((2,4-dihydroxyphenoxy)methyl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 
• 1416159-13-1 (2S,3R,4S,5R,6R)-2-(4-((2,4-bis(allyloxy)phenoxy)methyl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 
• 1416159-14-2 2,4-diallyloxyphenol 
• 1416159-11-9 (2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-(4-((2,4-bis(allyloxy)phenoxy)methyl)phenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 1400930-56-4 3-allyl-4-(allyloxy)-2-hydroxybenzaldehyde 
• 885687-10-5 4-(2,4-bis-allyloxy-benzyl)-6-hydroxymethyl-2-propyl-benzene-1,3-diol 
• 885687-06-9 5-(2,4-bis-allyloxy-benzyl)-2,4-dihydroxy-3-propyl-benzaldehyde 
• 885687-02-5 4-(2,4-bis-allyloxy-benzyl)-2-propyl-benzene-1,3-diol 

Relevant academic research and scientific papers

Use of o-hydroxy-p-methoxybenzaldehyde derivative as herbicide

The invention discloses an application of an o-hydroxy p-methoxybenzaldehyde derivative as a herbicide. The o-hydroxy-p-methoxybenzaldehyde derivative and the herbicide taking the o-hydroxy-p-methoxybenzaldehyde derivative as a component are used for preventing and removing weeds in a field crop growth place and a non-farming crop place.

Synthesis of benzodioxepanes

Four benzodioxepanes 1a-1d were prepared from reaction of 4-methoxy-3-hydroxybenzaldehyde 4 via a series of reasonable transformations, including the regioselective PhBCl2-mediated double allylation of 4, one-pot combination of ring-closing met

Synthesis of the parent resorcin[4]arene

The treatment of 2,4-bis(allyloxy)benzyl alcohols with Sc(OTf)3 in acetonitrile produced a cyclic tetramer as the major product, which was deallylated by ammonium formate and PdCl2(PPh3)2 to produce the parent r

Treatment and prophylaxis of diseases caused by parasites, or bacteria

Aromatic compounds, or prodrugs thereof, which contain an alkylating site and which are capable of alkylating the thiol group in N-acetyl-L-cysteine, in particular bis-aromatic α,β-unsaturated ketones, are used for the preparation of pharmaceutical compositions or medicated feed, food or drinking water for the treatment or prophylaxis of diseases caused by microorganisms or parasites, in particular protozoa such as Leishmannia, Trypanosoma, Toxoplasma, Plasmodium, Pneumocystis, Babesia and Theileria, intestinal protozoa such as Trichormionas and Ciardia; Coccidia such as Eimeria, Isospora, Cryptosporidium; Cappilaria, Microsporidium, Sarcocystis. Trichlodina, Trichoditella, Dacihylogurus, Pseudodacthylogurus, Acantocephalus, Ichthylophtherius, Botrecephalus; and intracellular bacteria, in particular Mycobacterium, Legionella species, Listeria and Salmonella. Preferred compounds have the formula (II): Xm --Ph--C(O)--CH=CH--Ph--Yn, wherein each phenyl group (Ph) may be mono- or polysubstituted; X and Y designate ARH or AZ, wherein A is O, S, NH or N(C1-6 alkyl), RH designates aliphatic hydrocarbyl, and Z is H or a masking group which is decomposed to liberate AH; m is 0, 1 or 2, and n is 0, 1, 2 or 3, whereby, when m is 2, then the two X are the same or different, and when n is 2 or 3, then the two or three Y are the same or different, with the proviso that n and m are not both 0. As examples of such compounds, chalcones, e.g. licochalcone A (obtainable i.a. from batches of Chinese licorice root of Glycyrrhiza species, e.g. G. uralensis or G. inflata) as well as hydroxy, alk(en)yl, and/or alk(en)yloxy analogues thereof are active in vitro and/or in vivo against i.a. L. major and P. falciparum.