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2-([3-[(2-hydroxyethoxy)methyl]phenyl]methoxy)ethanol is a complex organic compound with the molecular formula C13H18O5. It is a colorless liquid at room temperature and is soluble in water. This chemical is characterized by its unique structure, which includes a central phenyl ring with a methoxy group attached to the 3-position, and a 2-hydroxyethoxymethyl group attached to the same position. Additionally, there is a methoxy group attached to the 2-position of the phenyl ring, and a hydroxyl group at the 2-position of the terminal ethyl group. 2-([3-[(2-hydroxyethoxy)methyl]phenyl]methoxy)ethanol is used in various applications, such as in the synthesis of pharmaceuticals and as a chemical intermediate in the production of certain specialty chemicals. Its specific use and properties can vary depending on the context in which it is applied.

73636-41-6

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73636-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73636-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73636-41:
(7*7)+(6*3)+(5*6)+(4*3)+(3*6)+(2*4)+(1*1)=136
136 % 10 = 6
So 73636-41-6 is a valid CAS Registry Number.

73636-41-6Relevant academic research and scientific papers

COMPOUNDS AND USES THEREOF

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Page/Page column 313; 314, (2021/08/06)

The present disclosure features compounds and methods useful for the treatment of BAF complex-related disorders.

The Hantzsch 1,4-Dihydropyridine Synthesis as a Route to Bridged Pyridine and Dihydropyridine Crown Ethers

Kellogg, Richard M.,Bergen, T. J. van,Doren, Henk van,Hedstrand, David,Kooi, J.,et al.

, p. 2854 - 2862 (2007/10/02)

Mono-, di-, tri-, and tetraethylene glycols were transesterified with ethyl acetoacetate to give the bis(acetoacetate esters) 1a-d.On treatment of 1c,d with formaldehyde and excess (NH4)2CO3 in H2O a crude mixture of 1,4-dihydropyridines was obtained from which, after dehydrogenation to the pyridine form, the 3,5-bridged 2,6-dimethylpyridines 2c,d were isolated along with dimers 7c,d.Similar reaction of 1a gave only dimer 7a.The bridged pyridine 2d was methylated to give pyridinium salt 3d, which was reduced with Na2S2O4 to give 1,4-dihydropyridine 4d.Stable sodium salts of 4d and 6d were isolated.Bridged pyridines 10a-c substituted with, respectively, methyl, phenyl, and 2-furyl at the γ position of the pyridine ring have also been prepared, using 1d, (NH4)2CO3, and acetaldehyde, benzaldehyde, and 2-furfuraldehyde and Hantzsch condensation followed by dehydrogenation and chromatographic separation.Protection of the 1,3-dicarbonyl system of ethyl 4-bromo-3-oxobutanoate as its Na chelate followed by nucleophilic substitution with the bisalkoxides from tetra-, penta-, and hexaethylene glycols gave 4-substituted bis(acetoacetate esters) 16a-c.These on Hantzsch condensation yielded in low yield 2,6-bridged Hantzsch 1,4-dihydropyridines (17a-c).Treatment of 17a,b with alkali metal hydrides gave insoluble materials thought to be the internally solvated alkali metal salts of the (vinylogous) amide nitrogen of the 1,4-dihydropyridine.

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