87428-43-1

Basic information

• Product Name: Morpholine, 4-[(3,4-dimethoxyphenyl)thioxomethyl]-
• CAS NO: 87428-43-1
• Molecular Formula: C13H17NO3S
• Molecular Weight: 267.349
• Mol File: 87428-43-1.mol

Chemical Properties

• CAS DataBase Reference: Morpholine, 4-[(3,4-dimethoxyphenyl)thioxomethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Morpholine, 4-[(3,4-dimethoxyphenyl)thioxomethyl]-(87428-43-1)
• EPA Substance Registry System: Morpholine, 4-[(3,4-dimethoxyphenyl)thioxomethyl]-(87428-43-1)

Safety Data

• Hazardous Substances Data: 87428-43-1(Hazardous Substances Data)

Upstream product

• 952005-45-7 diphosphorus pentasulfide 
• 22792-13-8 4-(3’,4’-dimethoxybenzoyl)morpholine 
• 110-91-8 morpholine 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 1197285-84-9 C₁₄H₂₀NO₃S⁽¹⁺⁾*I^(1-) 
• 1215309-97-9 C₁₆H₁₅NO₅S 
• 428859-01-2 4-(4-chlorophenyl)-2-(3,4-dimethoxyphenyl)thiazole 
• 25020-85-3 2-(3,4-dimethoxyphenyl)-4-phenylthiazole 
• 1264748-29-9 C₁₂H₁₄O₃S 
• 1264748-28-8 C₂₂H₂₀O₃S 
• 1314692-82-4 C₁₁H₁₂O₅S 
• 111509-95-6 2-Cyano-3-(3,4-dimethoxyphenyl)-3-morpholinoacrylonitrile 
• 129852-39-7 4-Amino-3-(3,4-dimethoxyphenyl)pyrazolo<3,4-d>pyrimidine 
• 111510-06-6 5-Amino-3-(3,4-dimethoxyphenyl)-1H-pyrazole-4-carbonitrile 

Relevant articles and documents

Willgerodt-Kindler reaction at room temperature: Synthesis of thioamides from aromatic aldehydes and cyclic secondary amines

A simple method for the synthesis of thioamide derivatives in DMSO at room temperature and at 120 °C has been developed. Total 27 compounds were prepared under both conditions via a one-pot, three component reaction between substituted aromatic aldehydes,

Zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides: A new approach to the synthesis of amidines

The first zinc chloride catalyzed ring opening of N-arylsulfonyl aziridines by thioamides is described. Various thioamides were reacted with N-arylsulfonyl aziridines in the presence of a catalytic amount of dry zinc chloride to provide the corresponding

Efficient one-step synthesis of benzazoles in aqueous media

Benzazoles (benzoxazoles, benzothiazoles, and benzimidazoles) were efficiently prepared by the aquatic reaction of the corresponding thioamidinium salts and 2-aminophenol, 2-aminothiophenol, and 1,2-diaminobenzene, respectively. The thioamidinium salt was successfully applied as an alternative to a carboxylic acid derivative to react smoothly with an amino precursor and in the presence of catalytic amounts of hexadecyltrimethylammonium bromide salt to produce benzazoles in good to excellent yields. Wiley-VCH Verlag GmbH & Co. KGaA 2009.

Highly efficient synthesis of thioesters in water

Thioesters were efficiently prepared via the direct reaction of tertiary thioamides and alkyl halides in water, and in the presence of catalytic amounts of NaI, hexadecyltrimethylammonium bromide (HTAB), and 1,4-diazabicyclo[2.2.2] octane (DABCO). Hence,

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