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14950-55-1

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14950-55-1 Usage

General Description

1-(3,5-Dimethoxyphenyl)ethanol is a chemical compound with the molecular formula C10H14O3. It is a colorless liquid that is commonly used in the synthesis of pharmaceuticals and other organic compounds. This chemical is also known for its potential therapeutic properties, including anti-inflammatory and anti-cancer effects. It is often used as a precursor in the production of various pharmaceuticals and is known to have analgesic and anesthetic effects. Additionally, 1-(3,5-Dimethoxyphenyl)ethanol has been studied for its potential as a treatment for neurological disorders and is considered a promising candidate for further research in the field of medicine and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 14950-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,5 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14950-55:
(7*1)+(6*4)+(5*9)+(4*5)+(3*0)+(2*5)+(1*5)=111
111 % 10 = 1
So 14950-55-1 is a valid CAS Registry Number.

14950-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-Dimethoxyphenyl)ethanol

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:14950-55-1 SDS

14950-55-1Relevant articles and documents

Dynamic Kinetic Resolution of Alcohols by Enantioselective Silylation Enabled by Two Orthogonal Transition-Metal Catalysts

Oestreich, Martin,Seliger, Jan

supporting information, p. 247 - 251 (2020/10/29)

A nonenzymatic dynamic kinetic resolution of acyclic and cyclic benzylic alcohols is reported. The approach merges rapid transition-metal-catalyzed alcohol racemization and enantioselective Cu-H-catalyzed dehydrogenative Si-O coupling of alcohols and hydrosilanes. The catalytic processes are orthogonal, and the racemization catalyst does not promote any background reactions such as the racemization of the silyl ether and its unselective formation. Often-used ruthenium half-sandwich complexes are not suitable but a bifunctional ruthenium pincer complex perfectly fulfills this purpose. By this, enantioselective silylation of racemic alcohol mixtures is achieved in high yields and with good levels of enantioselection.

More than one kind of hydroxy phthalazine compound, preparation method and application thereof (by machine translation)

-

Paragraph 0027; 0028; 0030, (2017/09/01)

The invention belongs to the field of biomedical technology, in particular to more than one kind of hydroxy phthalazine compound, preparation method and application thereof, the polyhydroxylated phthalazine compounds of the chemical structure of general f

Metal-free trifluoromethylation of aromatic and heteroaromatic aldehydes and ketones

Qiao, Yupu,Si, Tuda,Yang, Ming-Hsiu,Altman, Ryan A.

, p. 7122 - 7131 (2014/08/18)

The ability to convert simple and common substrates into fluoroalkyl derivatives under mild conditions remains an important goal for medicinal and agricultural chemists. One representative example of a desirable transformation involves the conversion of aromatic and heteroaromatic ketones and aldehydes into aryl and heteroaryl β,β,β-trifluoroethylarenes and -heteroarenes. The traditional approach for this net transformation involves stoichiometric metals and/or multistep reaction sequences that consume excessive time, material, and labor resources while providing low yields of products. To complement these traditional strategies, we report a one-pot metal-free decarboxylative procedure for accessing β,β,β- trifluoroethylarenes and -heteroarenes from readily available ketones and aldehydes. This method features several benefits, including ease of operation, readily available reagents, mild reaction conditions, high functional-group compatibility, and scalability.

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