89332-92-3

Basic information

• Product Name: 2-Furancarbothioamide, N-methyl-
• Synonyms: 2-Furancarbothioamide,N-methyl;N-methyl-2-thiofuramide;N-methyl 2-furanecarbothioamide;furan-2-carbothioic acid methylamide;Furan-2-thiocarbonsaeure-methylamid
• CAS NO: 89332-92-3
• Molecular Formula: C6H7NOS
• Molecular Weight: 141.194
• Mol File: 89332-92-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 71-71.5 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 195.1±32.0 °C(Predicted)
• Density: 1.172±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Furancarbothioamide, N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarbothioamide, N-methyl-(89332-92-3)
• EPA Substance Registry System: 2-Furancarbothioamide, N-methyl-(89332-92-3)

Safety Data

• Hazardous Substances Data: 89332-92-3(Hazardous Substances Data)

Upstream product

• 6005-15-8 thiochromone 
• 41106-11-0 N-[2-furylmethylene]methanamine N-oxide 

Relevant articles and documents

SOME NOVEL ASPECTS OF REGIOSELECTIVITY IN 1,3 DIPOLAR CYCLOADDITIONS OF 4H-1-BENZOPYRAN-4-THIONE

4H-1-Benzopyran-4-thione (1) reacted smoothly with nitrilimines (3a-e) to afford regioselective cycloadducts (4a-e) in good yields.In contrast,benzonitrile oxide (6) and aldonitrones (7a-d) reacted preferentially at the thione function.The unstable cycloadduct (8) or (9) ruptured to give as isolable products chromone (10) and phenyl isothiocyanate (11) and the thioamides (12a-d).This indirectly proves the site of attack of the dipole at the thione group.