65057-97-8

Basic information

• Product Name: 2-(dimethoxymethyl)tetrahydro-2,5-dimethoxyfuran
• Synonyms: 2-(dimethoxymethyl)tetrahydro-2,5-dimethoxyfuran
• CAS NO: 65057-97-8
• Molecular Formula: C₉H₁₈O₅
• Molecular Weight: 206.23622
• EINECS: 265-329-6
• Mol File: 65057-97-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 255.6°C at 760 mmHg
• Flash Point: 95.2°C
• Appearance: /
• Density: 1.07g/cm³
• Vapor Pressure: 0.0259mmHg at 25°C
• Refractive Index: 1.437
• CAS DataBase Reference: 2-(dimethoxymethyl)tetrahydro-2,5-dimethoxyfuran(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(dimethoxymethyl)tetrahydro-2,5-dimethoxyfuran(65057-97-8)
• EPA Substance Registry System: 2-(dimethoxymethyl)tetrahydro-2,5-dimethoxyfuran(65057-97-8)

Safety Data

• Hazardous Substances Data: 65057-97-8(Hazardous Substances Data)

Usage

General Description

2-(dimethoxymethyl)tetrahydro-2,5-dimethoxyfuran is a chemical compound with the molecular formula C12H18O5. It is a derivative of tetrahydro-2,5-dimethoxyfuran, an organic compound containing a furan ring with two methoxy groups. The addition of a dimethoxymethyl group to the furan ring results in a compound with potential pharmaceutical and medicinal applications. The chemical structure and properties of 2-(dimethoxymethyl)tetrahydro-2,5-dimethoxyfuran make it a candidate for further research and development in the field of drug discovery and synthesis. Its unique combination of methoxy and furan groups may offer valuable insights for the design and synthesis of new pharmaceutical compounds with enhanced bioactivity and therapeutic potential.

InChI:InChI=1/C9H18O5/c1-10-7-5-6-9(13-4,14-7)8(11-2)12-3/h7-8H,5-6H2,1-4H3

Upstream product

• 1708-41-4 2-(furan-2-yl)-1,3-dioxolane 
• 59906-91-1 2,5-dihydro-2,5-dimethoxy-2-furaldehyde dimethyl acetal 

Downstream Products

• 1003-29-8 2-pyrrole aldehyde 
• 30186-39-1 N-phenylpyrrole-2-carbaldehyde 
• 1262333-07-2 1-(3,4-dimethoxybenzyl)-1,2,3,4,5,12b-hexahydropyrrolo-[2',1':3,4]pyrazino[1,2-a][1,3]diazepin-7(8H)-one 
• 1262333-06-1 1-benzyl-1,2,3,4,5,12b-hexahydropyrrolo[2',1':3,4]pyrazino[1,2-a][1,3]diazepin-7(8H)-one 
• 1262333-05-0 3,3-dimethyl-1-(3,4-dimethoxybenzyl)-1,3,4,11b-tetrahydro-2H-pyrrolo[2',1':3,4]pyrazino[1,2-a]pyrimidin-6(7H)-one 
• 1262333-02-7 1-(3,4-dimethoxybenzyl)-1,3,4,11b-tetrahydro-2H-pyrrolo-[2',1':3,4]-pyrazino[1,2-a]pyrimidin-6(7H)-one 
• 1262332-93-3 1-(3,4,5-trimethoxybenzyl)-1,2,3,10b-tetrahydroimidazo-[1,2-a]pyrrolo[2,1-c]pyrazin-5(6H)-one 
• 1262332-92-2 1-(3,4-dimethoxybenzyl)-1,2,3,10b-tetrahydroimidazo[1,2-a]-pyrrolo[2,1-c]pyrazin-5(6H)-one 
• 1262332-91-1 1-benzyl-1,2,3,10b-tetrahydroimidazo[1,2-a]pyrrolo[2,1-c]-pyrazin-5(6H)-one 
• 1095361-88-8 ethyl 2-(2-formyl-1H-pyrrol-1-yl)benzenecarboxylate 
• 79100-16-6 methyl 2-(2-formyl-1H-pyrrol-1-yl)benzenecarboxylate 
• 1095361-90-2 methyl 4,5-dimethoxy-2-(2-formyl-1H-pyrrol-1-yl)benzenecarboxylate 
• 1095362-25-6 C₂₄H₂₈N₂O₄ 
• 1095362-22-3 C₂₂H₂₄N₂O₂ 

Relevant articles and documents

On the formation of reductic acid from pentoses or hexuronic acids

Careful hydrolysis of (±)-cis- or (±)-trans-tetrahydro-2,5-dimethoxy-2-furaldehyde dimethyl acetal proceeded via 5,5-dimethoxy-4-oxopentanal to give (±)-trans-4-hydroxy-5-methoxy-2-cyclopenenone and (±)-trans-4,5-dihydroxy-2-cylopentenone. The latter product did not isomerize to 2,3-dihydroxy-2-cyclopentenone (reductic acid) on prolonged reaction. Careful hydrolysis of (±)-cis- or (±)-trans-tetrahydro-2, 5-dimethoxy-2-furaldehyde dimethyl acetal proceeded via 5, 5-dimethoxy-4-oxopentanal to give (±)-tran-4-hydroxy-5-methoxy-2-cyclopentenone and (±)-trans-4 ,5-dihydroxy-2-cyclopentenone. The latter product did not isomerize to 2,3-dihydroxy-2-cyclopentenone (reductic acid) on prolonged reaction.