6942-08-1 Usage
General Description
2-(2-methoxyethoxy)-1-phenylethanol, also known as Aromatic glycol GX, is a chemical compound that belongs to the class of glycol ethers. It is commonly used as a solvent in various industrial applications, including paints, coatings, and cleaning products. The chemical is a colorless liquid with a mild, pleasant odor and is considered to be relatively low in toxicity. It has the ability to dissolve a wide range of substances, making it versatile for use in different formulations. Additionally, it is known to have good stability and compatibility with other chemicals, making it a popular choice for many manufacturing processes.
Check Digit Verification of cas no
The CAS Registry Mumber 6942-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6942-08:
(6*6)+(5*9)+(4*4)+(3*2)+(2*0)+(1*8)=111
111 % 10 = 1
So 6942-08-1 is a valid CAS Registry Number.
6942-08-1Relevant academic research and scientific papers
Pyridine-directed organolithium addition to an enol ether
Yang, Jingyue,Dudley, Gregory B.
supporting information; experimental part, p. 3438 - 3442 (2011/02/24)
A previously reported anionic rearrangement of benzyl 2-pyridyl ethers can now be accessed by a distinct and unusual mechanism: addition of alkyllithium reagents to α-(2-pyridyloxy)-styrene triggers an anionic rearrangement to afford tertiary pyridyl carbinols. The process is explained by invoking a contra-electronic, pyridine-directed carbolithiation of the enol ether π-system. Copyright
A NEW AND SIMPLE SYNTHESIS OF ALKOXY- AND ARYLOXYMETHYLLITHIUM REAGENTS (ROCH2Li)
Corey, E. J.,Eckrich, Thomas M.
, p. 3163 - 3164 (2007/10/02)
A series of halomethyl alkyl and aryl ethers can be converted to the corresponding organolithium reagents (ROCH2Li) in a one-flask operation by sequential treatment (1) with stannous chloride-lithium bromide complex in tetrahydrofuran (THF) and (2) with n-butyllithium.
