Arasu, Mariadhas Valan et al. published their research in Industrial Crops and Products in 2019 | CAS: 3929-47-3

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).HPLC of Formula: 3929-47-3

Essential oil of four medicinal plants and protective properties in plum fruits against the spoilage bacteria and fungi was written by Arasu, Mariadhas Valan;Viayaraghavan, Ponnuswamy;Ilavenil, Soundarrajan;Al-Dhabi, Naif Abdullah;Choi, Ki Choon. And the article was included in Industrial Crops and Products in 2019.HPLC of Formula: 3929-47-3 This article mentions the following:

There are limited studies available regarding the chem. composition of essential oils and their activities against fruit spoilage bacteria and fungi. In this study, chem. composition of essential oils from medicinal plants namely Acorus calamus, Allium sativum, Mucuna pruriens, and Sesamum indicum L showed invitro antibacterial and antifungal properties against fruits spoilage microbes were evaluated. Gas Chromatograph-Mass Spectrometry anal. confirmed the presence of major metabolites namely Hydroxylamine (98.26%), 1,2,4 – trimethoxy-5-1-propenyl (93.07%), Dodecanoic acid, 1,2,3-propanetriyl ester (92.64) and 2-diisoprophylphosphinnoethane (67.97%) from the studied plants. The min. inhibitory concentration of the essential oils against bacteria were ranged from 11.3 ± 2.3 to 617 ± 4.9 μg/mL and fungi were ranged from 1.1 ± 0.4 to 292 ± 3.2 μg/mL, resp. Among the essential oil, Allium sativum showed significant antibacterial activity with least min. inhibitory concentration and min. bactericidal concentrations (11.3 ± 2.3 μg/mL and 24 ± 1.6 μg/mL) while Sesamum indicum oil showed the least activity with high min. inhibitory concentration and min. bactericidal concentrations values (460 ± 11.9 μg/mL and 940 ± 12.8 μg/mL). Interestingly, Allium sativum documented the highest antifungal activity against Penicillium notatum and also significantly inhibited the growth of other tested fungal species such as, Aspergillus niger, Aspergillus flavus and Rhizopus microsporus. Among all tested essential oils, in combination of studied antibiotics, essential oils from Allium sativum showed excellent synergistic activity against seven out of nine spoilage microbes. Two-way anal. of variance showed significant depletion of pathogenic microorganism due to the effect of essential oils (p < 0.05). In addition, essential oil from Allium sativum significantly reduced the growth of Aspertillus flavus and Aspergillus niger on plum fruit. Results revealed the application of essential oil from Allium sativum counter Aspergillus flavus growth and prevented deterioration of plum fruit. In the experiment, the researchers used many compounds, for example, 3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3HPLC of Formula: 3929-47-3).

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).HPLC of Formula: 3929-47-3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem