56583-59-6

Usage

Molecular Structure

1-Methoxy-6-Methyl-1.3-dihydrofuro[3.4-c]pyridin-7-ol is a complex organic compound with a pyridine derivative containing a furo-3.4-c-pyridine ring system.

Functional Groups

The compound has a methoxy group, a methyl group, and a hydroxyl group attached to the molecule.

Potential Applications

1-Methoxy-6-Methyl-1.3-dihydrofuro[3.4-c]pyridin-7-ol may have potential applications in pharmaceutical or medicinal chemistry due to its unique structure and functional groups.

Biological Activity

1-Methoxy-6-Methyl-1.3-dihydrofuro[3.4-c]pyridin-7-ol may possess biological activity or therapeutic potential.

Further Research

Additional research is likely needed to fully understand the properties and potential uses of 1-Methoxy-6-Methyl-1.3-dihydrofuro[3.4-c]pyridin-7-ol.

Upstream product

• 67-56-1 methanol 
• 65-22-5 pyridoxal hydrochloride 
• 66-72-8 pyridoxal 
• 77-78-1 dimethyl sulfate 
• 21634-26-4 pyridoxal hydrochloride 
• 74-88-4 methyl iodide 
• 868-85-9 Dimethyl phosphite 

Downstream Products

• 258531-75-8 3-trimethylmethylcarbonyl-6-{(E)-[2-(4-methoxycarbonyl)phenyl]ethenyl}pyridoxal monomethyl acetal 
• 258531-74-7 3-trimethylmethylcarbonyl-6-{(E)-[2-(4-methoxy)phenyl]ethenyl}pyridoxal monomethyl acetal 
• 258531-73-6 3-trimethylmethylcarbonyl-6-[(E)-(2-phenyl)ethenyl]pyridoxal monomethyl acetal 
• 258531-71-4 3-trimethylmethylcarbonyl-6-(phenyl)pyridoxal monomethylacetal 

Relevant academic research and scientific papers

Solvolysis of pyridoxal hydrochloride in alcohols

HPLC, 1H-NMR, MS and product analysis showed that pyridoxal hydrochloride was solvolyzed in methanol to form pyridoxal monomethylacetal. The reaction followed first order kinetics with the rate constant of 1.45 x 10-4 s-1 at 40 °C. The rate was not appreciably enhanced in the presence of an excess amount of HCl. The reaction was greatly retarded by addition of an equimolar amount of KOH. The results showed that the pyridinium-phenol species of pyridoxal hemiacetal is reactive. The reaction is responsible for the 'aging' of alcoholic solutions of pyridoxal, which has caused poor reproducibility of the kinetic data for the formation of Schiff bases with amino acids.

1-Alkoxy-7-hydroxy-1,3-dihydrofuro[3,4-c]pyridinium Salts

New salt structures have been synthesized from pyridoxal and various organic and inorganic acids.

Reaction of Pyridoxal with Hydrophosphoryl Compounds

The products of carbonyl phosphonylation of pyridoxal with dialkylphosphinous acid, alkylphosphinic acid ethyl esters, and phosphorous acid dialkyl (or diphenyl) esters have been obtained for the first time. In some cases, the products of addition are hyd

Versatile synthesis of 6-alkyl and aryl substituted pyridoxal derivatives

A versatile and convenient procedure for the functional derivatization with carbon substituents at the 6-position of pyridoxal using a Grignard reaction upon a protected N-isobutoxycarbonyloxypyridoxal chloride and Heck reactions with protected 6-vinylpyr

Pyridoxal Derivatives as Probes for Water Concentration in Non-aqueous Solvents

In order to provide a basis for the design of spectrofluorimetric indicators for water activity or concentration in organic solvents a series of O- and N-alkylated pyridoxal derivatives has been prepared.The compounds were examined for their ability to exhibit a shift in fluorescence emission wavelength on complexation with water.The shift in fluorescence on complexation with water previously observed (Yunxiang and Xin, Talanta, 1984, 31, 556) was confirmed for pyridoxal itself but alkylation of the oxygen functionalities blocked the fluorescence shift.In contrast, a strong enhancement in emission intensity but no shift in emission wavelength was observed with the N-methylpyridoxal.From these studies, it appears that modification at the nitrogen or, presumably, at C-2 or C-6 are the only available sites for the development of useful compounds from the pyridoxal prototype.