50634-05-4

Basic information

• Product Name: 2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE
• Synonyms: 2,5-DIMETHOXY-3-TETRAHYDROFURANCARBALDEHYDE;2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE;TIMTEC-BB SBB003968;2,5-Dimethoxy-3-tetrahydrofurancarboxaldehyde, mixture of isomers;tetrahydro-2,5-dimethoxyfuran-3-carbaldehyde;2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOX-AL DEHYDE, TECH., 90%, MIX. OF ISOMERS;2,5-Dimethoxy-3-tetrahydrofuranecarboxaldehyde;2,5-Dimethoxy-3-tetrahydrofurancarboxaldehyde, tech., mixture of isomers, 90%
• CAS NO: 50634-05-4
• Molecular Formula: C7H12O4
• Molecular Weight: 160.17
• EINECS: 256-668-0
• Product Categories: Building Blocks;Furans;Heterocyclic Building Blocks
• Mol File: 50634-05-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 89 °C12 mm Hg(lit.)
• Flash Point: 178 °F
• Appearance: Clear yellow to brown/Liquid
• Density: 1.129 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.232mmHg at 25°C
• Refractive Index: n20/D 1.4401(lit.)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE(50634-05-4)
• EPA Substance Registry System: 2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE(50634-05-4)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• Hazardous Substances Data: 50634-05-4(Hazardous Substances Data)

Usage

Description

2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE, also known as DMT-Furane, is an organic compound with the chemical formula C7H8O4. It is a clear yellow to brown liquid and is commonly used as a synthetic intermediate in the production of various chemical compounds.

Uses

Used in Pharmaceutical Industry:
2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE is used as a synthetic intermediate for the production of various pharmaceutical compounds. It plays a crucial role in the synthesis of 9-(3-formylpyrrol-1-yl) ester by reacting with ethyl 9-amino-4,5-dihydro-4-oxo-1,2,4-triazolo[1,5-a]quinoxaline-2-carboxylate, which can be further utilized in the development of novel therapeutic agents.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2,5-DIMETHOXY-3-TETRAHYDROFURANCARBOXALDEHYDE serves as a key building block for the creation of various complex organic molecules. Its unique structure and reactivity make it a valuable component in the synthesis of a wide range of compounds, including those with potential applications in various industries such as pharmaceuticals, agrochemicals, and materials science.

InChI:InChI=1/C7H12O4/c1-9-6-3-5(4-8)7(10-2)11-6/h4-7H,3H2,1-2H3/t5-,6+,7+/m0/s1

Upstream product

• 332-77-4 2,5-dihydro-2,5-dimethoxyfuran 
• 201230-82-2 carbon monoxide 

Downstream Products

• 143145-34-0 diethyl N-<4-(3-formyl-1-pyrrolyl)benzoyl>-L-glutamate 
• 120777-22-2 1-phenyl-1H-pyrrole-3-carbaldehyde 
• 691862-64-3 1-(3-fluoro-phenyl)-1H-pyrrole-3-carbaldehyde 
• 691862-62-1 1-(2-Fluoro-phenyl)-1H-pyrrole-3-carbaldehyde 
• 156496-64-9 1-[4-(trifluoromethyl)phenyl]-1H-pyrrole-3-carbaldehyde 
• 88075-88-1 1-(4-chlorophenyl)-1H-pyrrole-3-carbaldehyde 
• 864547-96-6 1-(2-methylphenyl)-1H-pyrrole-3-carbaldehyde 
• 288251-69-4 1-(4-fluorophenyl)-3-formylpyrrole 
• 117954-70-8 3-formyl-1-<(4-methylphenyl)sulfonyl>pyrrole 
• 126810-41-1 2-methyl-3-formyl-5-methoxytetrahydrofuran 
• 126810-43-3 2-phenyl-3-formyl-5-methoxytetrahydrofuran 
• 126810-44-4 2-phenylethynyl-3-formyl-5-methoxytetrahydrofuran 
• 30186-48-2 1-benzyl-1H-pyrrole-3-carbaldehyde 
• 897157-10-7 C₁₁H₇Cl₂NO 

Relevant articles and documents

LIQUID-PHASE HYDROFORMYLATION OF 2,3- AND 2,5-DIHYDROFURANS

The synthesis of 3-formyl derivatives of the tetrahydrofuran series was carried out by hydroformylation of 2,3-dihydrofuran and 2,5-dimethoxy-2,5-dihydrofuran in the presence of HRh(CO)(PPh3)3.The influence of the temperature, pressure, catalyst concentration, and the nature of the solvent on the conversion of dihydrofuran, the composition of aldehydes obtained and the selectivity of their formation was investigated.