639465-53-5

Basic information

• Product Name: 2-Furancarboxaldehyde, 4-(methylthio)- (9CI)
• Synonyms: 2-Furancarboxaldehyde, 4-(methylthio)- (9CI)
• CAS NO: 639465-53-5
• Molecular Formula: C6H6O2S
• Molecular Weight: 142.17564
• Product Categories: ALDEHYDE
• Mol File: 639465-53-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Furancarboxaldehyde, 4-(methylthio)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarboxaldehyde, 4-(methylthio)- (9CI)(639465-53-5)
• EPA Substance Registry System: 2-Furancarboxaldehyde, 4-(methylthio)- (9CI)(639465-53-5)

Safety Data

• Hazardous Substances Data: 639465-53-5(Hazardous Substances Data)

Upstream product

• 27065-51-6 2-(diethoxymethyl)-4-bromofuran 
• 21921-76-6 4-bromo-2-furancarbaldehyde 
• 639465-52-4 2-diethoxymethyl-4-methylthiofuran 

Downstream Products

• 349112-46-5 N-benzyl-N-[4-(methylsulfanyl)-2-furyl]methylamine 

Relevant articles and documents

IMINO SULFANONE INHIBITORS OF ENPP1

The present disclosure relates generally to inhibitors of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1), compositions thereof, and methods of using said compounds and compositions thereof. More specifically, the present disclosure relates to sulfoximine- based inhibitors of ENPP1 of Formula (I) and methods of their use for treating disease mediated by ENPP1.

Intra-molecular Diels-Alder reactions of citraconamic acids from furfurylamines and citraconic anhydride: Effects of substitution in the furan ring on regioselectivity

Regioselectivity in the intra-molecular Diels-Alder (IMDA) reaction of furfurylcitraconamic acids derived from N-benzylfurfurylamines and citraconic anhydride can be controlled by substituents located in the furan ring and by reaction conditions. Reactions conducted under kinetic conditions resulted in cycloaddition products having methyl and aminomethylene substituent in 1,3-relationship whereas under thermodynamic conditions, excepting in the case of the 3-methylsulfanyl group, the products rearranged to more stable cycloadducts in which the substituents are in 1,2-relationship. Product formation can be explained on the basis of frontier orbital interactions and steric considerations.