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Benzeneethanol, 4-(2-hydroxyethoxy)-, also known as Phenoxyethanol, is a widely used organic compound with the chemical formula C8H10O2. It is a colorless, viscous liquid that is soluble in water and has a mild, pleasant odor. Phenoxyethanol is commonly used as a preservative in cosmetics, pharmaceuticals, and personal care products due to its antimicrobial properties. It is effective against a broad range of microorganisms, including bacteria, yeasts, and molds, and is considered safe for use in these applications. The compound is also used as a solvent and a stabilizer in various industrial processes.

4960-67-2

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4960-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4960-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4960-67:
(6*4)+(5*9)+(4*6)+(3*0)+(2*6)+(1*7)=112
112 % 10 = 2
So 4960-67-2 is a valid CAS Registry Number.

4960-67-2Downstream Products

4960-67-2Relevant academic research and scientific papers

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

, p. 4747 - 4753 (2014)

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

ADHESIVE BONDING COMPOSITION AND USE THEREOF

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Page/Page column 53; 57; 58, (2015/09/23)

An adhesive dental composition comprising apolymerizable monomer (1), a polymerizable monomer (2) comprising an acidic moiety,initiator component(s), filler component(s) in an amount of less than about 15 wt.-%, wt.-% with respect to the whole weight of t

DENTAL COMPOSITION AND USE THEREOF

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Page/Page column 60; 64; 65, (2015/09/28)

The invention relates to a dental composition comprising polymerizable monomer (1), initiator component(s), filler component(s) in an amount of more than about 20 wt.-%, wt.-% with respect to the whole weight of the composition, the polymerizable monomer

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