159551-33-4

Basic information

• Product Name: 3-Furancarboxaldehyde, tetrahydro-2,5-dimethoxy-, [2R-(2alpha,3beta,5beta)]- (9CI)
• Synonyms: 3-Furancarboxaldehyde, tetrahydro-2,5-dimethoxy-, [2R-(2alpha,3beta,5beta)]- (9CI)
• CAS NO: 159551-33-4
• Molecular Formula: C7H12O4
• Molecular Weight: 160.16778
• Product Categories: ALDEHYDE
• Mol File: 159551-33-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 206.9±0.0 °C(Predicted)
• Appearance: /
• Density: 1.11±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 3-Furancarboxaldehyde, tetrahydro-2,5-dimethoxy-, [2R-(2alpha,3beta,5beta)]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Furancarboxaldehyde, tetrahydro-2,5-dimethoxy-, [2R-(2alpha,3beta,5beta)]- (9CI)(159551-33-4)
• EPA Substance Registry System: 3-Furancarboxaldehyde, tetrahydro-2,5-dimethoxy-, [2R-(2alpha,3beta,5beta)]- (9CI)(159551-33-4)

Safety Data

• Hazardous Substances Data: 159551-33-4(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 1392287-87-4 (3-(3-carbamoyl-1H-pyrrol-1-yl)phenoxycarbonyl)(2-(2-(2-fluorophenoxy)ethoxy)ethyl)amine 
• 1392287-89-6 (3-(3-carbamoyl-1H-pyrrol-1-yl)phenoxycarbonyl)(2-(2-(2,4-difluorophenoxy)ethoxy)ethyl)amine 
• 1392287-91-0 (3-(3-carbamoyl-1H-pyrrol-1-yl)phenoxycarbonyl)(2-(2-(2,4,6-trifluorophenoxy)ethoxy)ethyl)amine 
• 1392288-24-2 1-(3-hydroxyphenyl)-1H-pyrrole-3-carbonitrile 
• 1245740-12-8 1-(3-hydroxyphenyl)-1H-pyrrole-3-carboxamide 
• 1245740-11-7 1-(3-hydroxyphenyl)-1H-pyrrole-3-carboxylic acid 
• 1245740-27-5 undec-10-ynyl-1-(3-hydroxyphenyl)-1H-pyrrole-3-carboxylate 
• 1245740-28-6 6-phenylhexyl-1-(3-hydroxyphenyl)-1H-pyrrole-3-carboxylate 
• 1245739-96-1 ST₃₉₁₀ 
• 1245739-98-3 ST₃₉₁₂ 
• 1245739-97-2 ST₃₉₁₁ 
• 1245740-06-0 ST₄₁₁₂ 
• 1417454-18-2 C₂₀H₂₄N₄O₂ 
• 1417454-16-0 C₁₅H₁₆N₄ 

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.