31646-31-8

Basic information

• Product Name: Morpholinium, 4-[[4-(dimethylamino)phenyl](methylthio)methylene]-,iodide
• CAS NO: 31646-31-8
• Molecular Formula: C14H21N2OS.I
• Molecular Weight: 392.304
• Mol File: 31646-31-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Morpholinium, 4-[[4-(dimethylamino)phenyl](methylthio)methylene]-,iodide(CAS DataBase Reference)
• NIST Chemistry Reference: Morpholinium, 4-[[4-(dimethylamino)phenyl](methylthio)methylene]-,iodide(31646-31-8)
• EPA Substance Registry System: Morpholinium, 4-[[4-(dimethylamino)phenyl](methylthio)methylene]-,iodide(31646-31-8)

Safety Data

• Hazardous Substances Data: 31646-31-8(Hazardous Substances Data)

Upstream product

• 74-88-4 methyl iodide 
• 5925-53-1 4-<4-(Dimethylamino)thiobenzoyl>morpholine 

Downstream Products

• 100-10-7 4-dimethylamino-benzaldehyde 
• 111997-60-5 2-(2-hydroxyphenyl)-5-(4-dimethylaminophenyl)-1,3,4-oxadiazole 
• 1874-35-7 2-(N,N-dimethyl-4-aminophenyl)-5-phenyl-1,3,4-oxadiazole 
• 120290-15-5 Dimethyl-[4-(methylsulfanyl-morpholin-4-yl-methyl)-phenyl]-amine 
• 31646-11-4 4-<4-(Dimethylamino)selenobenzoyl>morpholine 
• 118792-43-1 S-methyl 4-(dimethylamino)benzothioate 
• 904817-05-6 C₁₆H₁₅N₃O₂ 
• 10205-56-8 2-(4-N,N-dimethylaminophenyl)benzothiazole 
• 840-57-3 2-(p-dimethylaminophenyl)benzoxazole 
• 2562-71-2 2-(4-dimethylaminophenyl)-1H-benzimidazole 

Relevant articles and documents

Solvent-free conversion of thioamides to thioesters

Diverse thioesters were efficiently prepared via the solvent-free reaction of thioamide derivatives with alkyl halides in the presence of catalytic amounts of 1,4-diazabicyclo[2.2.2]octane (DABCO) in small quantities of water and in good to excellent yiel

HIGHLY COORDINATE ORGANOSILICON COMPOUNDS IN SYNTHESIS: NEW ENTRY TO S,N-ACETALS BY SELECTIVE REDUCTION OF ALKYLTHIOMETHYLENIMINIUM SALTS BY USE OF TRIMETHOXYSILANE AND DILITHIUM 2,3-BUTANDIOLATE

Reduction of alkylthiomethyleniminium iodides proceeds smoothly by use of trimethoxysilane and dilithium 2,3-butandiolate in tetrahydrofuran at 0 deg C to give the corresponding S,N-acetals selectively in high yield.