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5653-65-6

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5653-65-6 Usage

General Description

1-(3,4-Dimethoxyphenyl)ethanol is a chemical compound with the molecular formula C10H14O3. It belongs to the family of phenyl ethanols and is primarily used in the production of pharmaceuticals and fragrances. The compound is a colorless liquid with a mild, floral odor, and it is insoluble in water but soluble in organic solvents. Its primary function in pharmaceuticals is as an intermediate in the synthesis of various drugs, while in the fragrance industry, it is used as a scent additive. Additionally, it has been studied for its potential use in antifungal and antimicrobial applications. Overall, 1-(3,4-Dimethoxyphenyl)ethanol is a versatile compound with a range of industrial and potential medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5653-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5653-65:
(6*5)+(5*6)+(4*5)+(3*3)+(2*6)+(1*5)=106
106 % 10 = 6
So 5653-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O3/c1-7(11)8-4-5-9(12-2)10(6-8)13-3/h4-7,11H,1-3H3

5653-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-Dimethoxyphenyl)ethanol

1.2 Other means of identification

Product number -
Other names 1-(3,4-DIMETHOXYPHENYL)ETHANOL

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:5653-65-6 SDS

5653-65-6Relevant articles and documents

Miscibility and hydrogen bonding in blends of poly(ethylene oxide) and kraft lignin

Kadla, John F.,Kubo, Satoshi

, p. 7803 - 7811 (2003)

Polymer blending is a convenient method to develop products with desirable properties. Through specific intermolecular interactions favorable polymer blending can occur, and composite materials with desirable properties can be produced. In this study we h

Nickel-Catalyzed Enantioselective Hydroboration of Vinylarenes

Tran, Hai N.,Stanley, Levi M.

supporting information, p. 395 - 399 (2021/12/27)

The enantioselective hydroboration of vinylarenes catalyzed by a chiral, nonracemic nickel catalyst is presented as a facile method for generating chiral benzylic boronate esters. Various vinylarenes react with bis(pinacolato)diboron (B2pin2) in the presence of MeOH as a hydride source to form chiral boronate esters in up to 92% yield with up to 94% ee. The use of anhydrous Me4NF to activate B2pin2 is crucial for ensuring fast transmetalation to achieve high enantioselectivities.

Ambient-pressure highly active hydrogenation of ketones and aldehydes catalyzed by a metal-ligand bifunctional iridium catalyst under base-free conditions in water

Wang, Rongzhou,Yue, Yuancheng,Qi, Jipeng,Liu, Shiyuan,Song, Ao,Zhuo, Shuping,Xing, Ling-Bao

, p. 1 - 7 (2021/05/17)

A green, efficient, and high active catalytic system for the hydrogenation of ketones and aldehydes to produce corresponding alcohols under atmospheric-pressure H2 gas and ambient temperature conditions was developed by a water-soluble metal–ligand bifunctional catalyst [Cp*Ir(2,2′-bpyO)(OH)][Na] in water without addition of a base. The catalyst exhibited high activity for the hydrogenation of ketones and aldehydes. Furthermore, it was worth noting that many readily reducible or labile functional groups in the same molecule, such as cyan, nitro, and ester groups, remained unchanged. Interestingly, the unsaturated aldehydes can be also selectively hydrogenated to give corresponding unsaturated alcohols with remaining C=C bond in good yields. In addition, this reaction could be extended to gram levels and has a large potential of wide application in future industrial.

Highly efficient Meerwein-Ponndorf-Verley reductions over a robust zirconium-organoboronic acid hybrid

Song, Jinliang,Hua, Manli,Huang, Xin,Visa, Aurelia,Wu, Tianbin,Fan, Honglei,Hou, Minqiang,Zhang, Zhaofu,Han, Buxing

, p. 1259 - 1265 (2021/02/26)

The Meerwein-Ponndorf-Verley (MPV) reaction is an attractive approach to selectively reduce carbonyl groups, and the design of advanced catalysts is the key for these kinds of interesting reactions. Herein, we fabricated a novel zirconium organoborate using 1,4-benzenediboronic acid (BDB) as the precursor for MPV reduction. The prepared Zr-BDB had excellent catalytic performance for the MPV reduction of various biomass-derived carbonyl compounds (i.e., levulinate esters, aldehydes and ketones). More importantly, the number of borate groups on the ligands significantly affected the catalytic activity of the Zr-organic ligand hybrids, owing to the activation role of borate groups on hydroxyl groups in the hydrogen source. Detailed investigations revealed that the excellent performance of Zr-BDB was contributed by the synergetic effect of Zr4+and borate. Notably, this is the first work to enhance the activity of Zr-based catalysts in MPV reactions using borate groups.

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