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5406-14-4

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5406-14-4 Usage

General Description

3,5-xylyloxyacetic acid is a chemical compound with the molecular formula C10H12O4 and a molecular weight of 196.2 g/mol. It is a derivative of acetic acid and contains a xylyloxy moiety, which consists of a xylyl group attached to an oxygen atom. 3,5-xylyloxyacetic acid is commonly used as a building block in the synthesis of various organic compounds and can be employed in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It has also been investigated for its potential use as a corrosion inhibitor for metal surfaces. 3,5-xylyloxyacetic acid is a solid substance that is soluble in organic solvents but insoluble in water. It may pose health risks if inhaled, ingested, or brought into contact with the skin, and appropriate safety precautions should be taken when handling this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 5406-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5406-14:
(6*5)+(5*4)+(4*0)+(3*6)+(2*1)+(1*4)=74
74 % 10 = 4
So 5406-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-7-3-8(2)5-9(4-7)13-6-10(11)12/h3-5H,6H2,1-2H3,(H,11,12)/p-1

5406-14-4SDS

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 2-(3,5-dimethylphenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names O-(3.5-Dimethyl-phenyl)-glykolsaeure

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:5406-14-4 SDS

5406-14-4Relevant articles and documents

INHIBITORS TO TARGET HIV-1 NEF-CD80/CD86 INTERACTIONS FOR THERAPEUTIC INTERVENTION

-

, (2020/03/05)

The compounds of Formula I, II, and III along with their stereoisomers, pharmaceutically acceptable salts, polymorphs, solvates and hydrates thereof are described in the present disclosure. The said compounds restore immune activation in case of infections or a disease associated with an HIV infection in a subject in need thereof.

Copper(ii)-catalyzed C-O coupling of aryl bromides with aliphatic diols: Synthesis of ethers, phenols, and benzo-fused cyclic ethers

Liu, Yajun,Park, Se Kyung,Xiao, Yan,Chae, Junghyun

supporting information, p. 4747 - 4753 (2014/06/24)

A highly efficient copper-catalyzed C-O cross-coupling reaction between aryl bromides and aliphatic diols has been developed employing a cheaper, more efficient, and easily removable copper(ii) catalyst. A broad range of aryl bromides were coupled with aliphatic diols of different lengths using 5 mol% CuCl2 and 3 equivalents of K2CO3 in the absence of any other ligands or solvents to afford the corresponding hydroxyalkyl aryl ethers in good to excellent yields. In this newly developed protocol, aliphatic diols have multilateral functions as coupling reactants, ligands, and solvents. The resulting hydroxyalkyl aryl ethers were further readily converted into the corresponding phenols, presenting a valuable alternative way to phenols from aryl bromides. Furthermore, it was demonstrated that they are useful intermediates for more advanced molecules such as benzofurans and benzo-fused cyclic ethers. This journal is

Copper(II)-catalyzed hydroxylation of aryl halides using glycolic acid as a ligand

Xiao, Yan,Xu, Yongnan,Cheon, Hwan-Sung,Chae, Junghyun

, p. 5804 - 5809 (2013/07/25)

Copper(II)-catalyzed hydroxylation of aryl halides has been developed to afford functionalized phenols. The protocol utilizes the reagent combination of Cu(OH)2, glycolic acid, and NaOH in aqueous DMSO, all of which are cheap, readily available, and easily removable after the reaction. A broad range of aryl iodides and activated aryl bromides were transformed into the corresponding phenols in excellent yields. Moreover, it has been shown that C-O(alkyl)-coupled product, instead of phenol, can be predominantly formed under similar reaction conditions.

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