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2-(3-methoxyphenoxy)-1-phenylethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29509-27-1

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29509-27-1 Usage

Type of compound

Phenolic compound

Structure

Contains a phenyl ring and an ethane backbone with a hydroxyl group

Usage in perfumes and cosmetics

Acts as a fragrance ingredient due to its pleasant aroma

Pharmaceutical applications

Possesses antioxidant and anti-inflammatory properties

Organic synthesis

Can be used as a reagent to form various derivatives and analogues

Industrial and scientific applications

Benefits from its unique chemical structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 29509-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,0 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29509-27:
(7*2)+(6*9)+(5*5)+(4*0)+(3*9)+(2*2)+(1*7)=131
131 % 10 = 1
So 29509-27-1 is a valid CAS Registry Number.

29509-27-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxyphenoxy)-1-phenylethanol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29509-27-1 SDS

29509-27-1Downstream Products

29509-27-1Relevant academic research and scientific papers

Cleavage∕cross-coupling strategy for converting β-O-4 linkage lignin model compounds into high valued benzyl amines via dual C–O bond cleavage

Jia, Le,Li, Chao-Jun,Zeng, Huiying

, (2021/10/29)

Lignin is the most recalcitrant of the three components of lignocellulosic biomass. The strength and stability of the linkages have long been a great challenge for the degradation and valorization of lignin biomass to obtain bio-fuels and commercial chemicals. Up to now, the selective cleavage of C–O linkages of lignin to afford chemicals contains only C, H and O atoms. Our group has developed a cleavage/cross-coupling strategy for converting 4-O-5 linkage lignin model compounds into high value-added compounds. Herein, we present a palladium-catalyzed cleavage/cross-coupling of the β-O-4 lignin model compounds with amines via dual C–O bond cleavage for the preparation of benzyl amine compounds and phenols.

Intervening Bismuth Tungstate with DNA Chain Assemblies: A Perception toward Feedstock Conversion via Photoelectrocatalytic Water Splitting

Bandla, Nischala,Kumar, M. Praveen,Kumaravel, Sangeetha,Kundu, Subrata,Ravichandran, Subbiah,Sankar, Selvasundarasekar Sam,Thiruvengetam, Prabaharan

supporting information, p. 14501 - 14512 (2020/10/12)

An advanced approach with DNA-mediated bismuth tungstate (Bi2WO6) one-dimensional (1-D) nanochain assemblies for hydrogen production with 5-fold enhanced photoelectrochemical (PEC) water splitting reaction is presented. The creation of new surface states upon DNA modification mediates the electron transfer in a facile manner for a better PEC process. The UV-Vis-DRS analysis results a red shift in the optical absorption phenomenon with the interference of DNA modification on Bi2WO6, and, thus, the band gap was tuned from 3.05 eV to 2.71 eV. The applied bias photon-to-current efficiency (ABPE) was calculated and shows a maximum for the Bi2WO6?DNA-2 (25.22 × 10-4%), compared to pristine Bi2WO6 (7.76 × 10-4%). Furthermore, the idea of practical utility of produced hydrogen from PEC is established for the first time with photocatalytic feedstock conversion to platform chemicals using cinnamaldehyde, 2-hydroxy-1-phenylethanone, and 2-(3-methoxyphenoxy)-1-phenylethanone in large scale by hydrogenation and/or hydrogenolysis reactions under eco-friendly green conditions with external hydrogen pressure in an aqueous mixture. Also, the recyclability experiment delivered good yields, which further confirm the robustness of the developed catalyst.

Tuning Cu Overvoltage for a Copper-Telluride System in Electrocatalytic Water Reduction and Feasible Feedstock Conversion: A New Approach

Johny, Jinta Merlin,Karthick, Kannimuthu,Kumaravel, Sangeetha,Kundu, Subrata,Sankar, Selvasundarasekar Sam,Thiruvengetam, Prabaharan

supporting information, (2020/08/12)

Highly efficient and earth-abundant elements capable of water reduction by electrocatalysis and are attractive for the sustainable generation of fuels. Among the earth-abundant metals, copper is one of the cheapest but often the most neglected choice for the hydrogen evolution reaction (HER) due to its high overvoltage. Herein, for the first time we have tuned the overpotential of copper by tellurizing it by two different methodologies, viz. hydrothermal and wet chemical methods, which form copper telluride nanochains and aggregates. The application of copper telluride as an electrocatalyst for the HER gave fruitful results in terms of both activity and stability. The hydrothermally synthesized catalyst Cu2-xTe/hyd shows a low overpotential (347 mV) at 10 mA cm-2 toward the HER. In addition, the catalyst showed a very low charge transfer resistance (Rct) of 24.4 ω and, as expected, Cu2-xTe/hyd exhibited a lower Tafel slope value of 188 mV/dec in comparison to Cu2-xTe/wet (280 mV/dec). A chronoamperometry study reveals the long-term stability of both catalysts even up to 12 h. The Faradaic efficiency of Cu2-xTe/hyd was calculated and found to be 95.06percent by using gas chromatographic (GC) studies. Moreover, with the idea of utilizing produced hydrogen (H2) from electrocatalysis, for the first time we have carried out feedstock conversion to platform chemicals in water under eco-friendly green conditions. We have chosen cinnamaldehyde, 2-hydroxy-1-phenylethanone, 4-(benzyloxy)benzaldehyde, and 2-(3-methoxyphenoxy)-1-phenylethanone (β-O-4) as model compounds for feedstock conversion by hydrogenation and/or hydrogenolysis reactions in aqueous medium using external hydrogen pressure. This protocol could also be scaled up for large-scale conversion and the catalyst is likely to find industrial application since it requires an inexpensive catalyst and an easily available, mild reducing agent. The robustness of the developed catalyst is proven by recyclability experiments and its possibility of use in real-life applications.

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