6280-98-4

Usage

Uses

Used in Chemical Synthesis:
1,2-Di-N-Propoxybenzene is used as an intermediate in the synthesis of various chemical compounds for industrial applications. Its propoxy functional groups allow for further reactions and modifications, making it a versatile building block in the chemical industry.
Used in Industrial Applications:
1,2-Di-N-Propoxybenzene is used as a component in the production of certain industrial products. Its aromatic ether structure provides specific properties that may be desirable in certain applications, such as solvents, plasticizers, or other specialty chemicals.
Note: Due to the lack of detailed information on the physical properties, toxicity, and specific industrial applications of 1,2-Di-N-Propoxybenzene, it is essential to handle 1,2-DI-N-PROPOXYBENZENE with caution until comprehensive safety data is available.

Upstream product

• 120-80-9 benzene-1,2-diol 
• 106-94-5 propyl bromide 
• 4218-87-5 1,2-bis-allyloxy-benzene 

Downstream Products

• 100620-61-9 4-chloromethyl-1,2-dipropoxy-benzene 
• 85417-84-1 4-bromo-1,2-bis(propoxy)benzene 
• 127119-34-0 4-propionyl-1,2-dipropoxybenzene 
• 123769-54-0 (E)-1-(3,4-Dipropoxy-phenyl)-3-phenyl-propenone 
• 123769-53-9 (3,4-Dipropoxy-phenyl)-phenyl-methanone 
• 105321-59-3 1,2-dipropoxy-4-acetylbenzene 
• 50766-19-3 1,6-Bis-(3,4-dipropoxyphenyl)-1,6-hexandion 
• 118464-38-3 1,2-dibromo-4,5-dipropyloxybenzene 
• 101114-73-2 3,4-dipropoxy-benzyl thiocyanate 
• 69769-43-3 (3,4-dipropoxy-phenyl)-acetonitrile 
• 161199-97-9 1,2-dipropoxy-4-(3-dimethylaminopropionyl)benzene 
• 86723-15-1 1,2-dipropyloxy-4,5-diaminobenzene 
• 33332-61-5 1,2-dipropoxy-4,5-dinitrobenzene 
• 91645-47-5 4-Nitro-1,2-dipropoxy-benzene 

Relevant academic research and scientific papers

Synthesis of Armchair and Chiral Carbon Nanobelts

Carbon nanobelts that consist of a loop of fully fused benzene rings are long-standing and challenging targets of organic synthesis and are key steps toward the ultimate synthesis of uniform carbon nanotubes (CNTs) of single chirality and predefined diame

Unexpected beauty and diversity in the structures of three homologous 4,5-dialkoxy-1-ethynyl-2-nitrobenzenes: The subtle interplay between intermolecular C - H...O hydrogen bonds and alkyl chain length

The synthesis, 1H and 13C NMR spectra, and X-ray structures are described for three dialkoxy ethynylnitrobenzenes that differ only in the length of the alkoxy chain, namely 1-ethynyl-2-nitro-4,5-dipropoxybenzene, C14H

METHODS AND COMPOSITIONS FOR CONTROL OF GYPSY MOTHS, Lymanria dispar

The invention provides in part dialkoxybenzene and eugenol compounds for controlling infestation by a Lymantria dispar, and methods thereof. The compounds include a compound of Formula I: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; R2 may be at positions 2, 3 or 4 and may be H, methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; and R3 may be optionally present at positions 2, 3 and 4, and is allyl; with the provisos that when R2 is at position 2, R3 if present is at position 3, or when R2 is at to position 3, R3 if present is at positions 2 or 4, or when R2 is at position 4, R3 if present is at position 2; or of Formula II: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; or mixtures thereof.

METHODS AND COMPOSITIONS FOR CONTROL OF CABBAGE LOOPER, Trichoplusia ni

The invention provides in part dialkoxybenzene compounds for controlling infestation by a Trichoplusia ni, and methods thereof. The compounds include a compound of Formula I: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl(3-methylbutyl) or allyl; R2 may be at positions 2, 3 or 4 and may be H, methyl, ethyl, propyl, n-butyl, isopentyl(3-methylbutyl) or allyl; and R3 may be optionally present at positions 2, 3 and 4, and is allyl; except that when R2 is at position 2, R3 if present is at position 3, and when R2 is at position 3, R3 if present is at positions 2 or 4, and when R2 is at position 4, R3 if present is at position 2, and when R2 is at position 4 and R3, if present, has reacted with an OH group at position 1 in a Markovnikov sense, then R3 becomes R4, a dihydrofuran.

Photophysical and photochemical properties of fluorinated and nonfluorinated n-Propanol-substituted zinc phthalocyanines

The synthesis of symmetrical fluorinated and nonfluorinated zinc(II) phthalocyanine derivatives obtained from. 4,5-dichlorophthalonitrile, 4-nitrophthalonitrile and 3-nitrophthalonitrile substituted with 2,2,3,3-tetrafluoro-1-propanol and npropanol are de

Screening of dialkoxybenzenes and disubstituted cyclopentene derivatives against the cabbage looper, Trichoplusia ni, for the discovery of new feeding and oviposition deterrents

The antifeedant, oviposition deterrent, and toxic effects of dialkoxybenzene minilibraries and of disubstituted cyclopentene minilibraries (i.e., consisting of four to five compounds) along with their pure constituent compounds were assessed against third instar larvae and adults of the cabbage looper, Trichoplusia ni, in laboratory bioassays in a search for new insect control agents. These compounds mimic naturally occurring bioactive odorants and tastants and are relatively easily prepared from commodity chemicals. Most of these libraries strongly deterred larval feeding, with some exhibiting strong toxic and oviposition deterrent effects as well. Our results suggest some structure-function relationships within these libraries. Replacement of a methyl group with larger alkyl substituents increased the feeding deterrent effects in most cases. The presence of a free hydroxyl group, irrespective of the carbon framework or alkyl substituent, served to reduce feeding deterrent effects in all series of compounds. Further, exceeding a certain group size also generally had a detrimental effect. This information will be useful in designing new insect control agents for agriculture. Some of these libraries and compounds may have potential for development as commercial insecticides.

Palladium Nanoparticles in Polymers: Catalyst for Alkene Hydrogenation, Carbon-Carbon Cross-Coupling Reactions, and Aerobic Alcohol Oxidation

A new recyclable palladium catalyst was synthesized by a simple procedure from readily available reagents, which is composed of palladium nanoparticles dispersed in an organic polymer. This catalyst is robust, and highly active in many organic transformations including alkene and alkyne hydrogenation, carbon-carbon cross-coupling reactions, and aerobic alcohol oxidation.

Synthesis and specific features of mesomorphic behavior of new polysubstituted triphenylenes

Previously unknown 2,3,6,7,10,11-hexakis(dodecyloxy)triphenylene and -(tetradecyloxy)triphenylene were synthesized. The structures of the synthesized compounds were proved by elemental analysis and spectral methods. Polymesomorphism was found for the first time and studied for substances of the hexaalkoxytriphenylene homologic series, as well as liotropic mesomorphism in a series of organic solvents.

The polymer incarcerated method for the preparation of highly active heterogeneous palladium catalysts

A new method named "the polymer incarcerated (PI) method" for preparing a heterogeneous palladium catalyst has been developed. The method is operationally simple, and the Pd catalyst prepared (PI Pd) is highly active for hydrogenation, carbon-carbon, and carbon-oxygen bond-forming reactions. Remarkable points are that the activity of PI Pd is higher than that of homogeneous Pd catalysts and that PI Pd is recovered by simple filtration and reused several times without loss of activity. The catalyst is expected to replace many heterogeneous palladium catalysts, especially Pd/C, which is often used in academia and industry, but recovery of which is difficult. Copyright

Rapid synthesis of new discotic liquid crystals based on diquinoxalino[2,3-a:2′,3′-c]phenazine containing hexakis(alkoxy) side arms

The condensation of 1,2-bisalkoxy-4,5-diaminobenzene 2a-e derivatives with freshly prepared hexaketocyclohexane give hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′-c]phenazines in good yield. DSC and polarization microscopy showed HATOC6 has both the crystalline (K) to mesophase (M) and the mesophase (M) to isotropic (I) phase transitions. Importantly, the alkoxy substituted compound synthesized showed an M-I transition because of greater stability, whereas the reported alkyl-thiol decomposes after the mesophase.