15482-63-0

Basic information

• Product Name: Benzenecarbothioamide, 4-methoxy-N,N-dimethyl-
• CAS NO: 15482-63-0
• Molecular Formula: C10H13NOS
• Molecular Weight: 195.285
• Mol File: 15482-63-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzenecarbothioamide, 4-methoxy-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarbothioamide, 4-methoxy-N,N-dimethyl-(15482-63-0)
• EPA Substance Registry System: Benzenecarbothioamide, 4-methoxy-N,N-dimethyl-(15482-63-0)

Safety Data

• Hazardous Substances Data: 15482-63-0(Hazardous Substances Data)

Upstream product

• 104-47-2 p-methoxybenzylnitrile 
• 68-12-2 N,N-dimethyl-formamide 
• 123-11-5 4-methoxy-benzaldehyde 
• 105-13-5 4-Methoxybenzyl alcohol 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 824-94-2 p-methoxybenzyl chloride 
• 7291-00-1 N,N-dimethyl-4-methoxybenzamide 
• 768-60-5 4-methoxyphenylacetylen 
• 5925-50-8 O-methyl 4-methoxybezenecarbothioate 
• 136992-18-2 (4-Methoxy-phenyl)-methylselanyl-methanethione 
• 124-40-3 dimethyl amine 
• 506-59-2 N,N-dimethylammonium chloride 
• 100-66-3 methoxybenzene 
• 16420-13-6 N,N-Dimethylthiocarbamoyl chloride 

Downstream Products

• 36358-12-0 2-ethoxy-2-(4-methoxy-phenyl)-3,5-diphenyl-2,3-dihydro-[1,3,4]thiadiazole 
• 95213-52-8 C₁₁H₁₆N₄OS 
• 95213-61-9 4-Methoxy-N,N-dimethyl-N'-methylsulfanyl-benzamidine 

Relevant articles and documents

Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides

An improved and efficient method for the synthesis of thioamides is presented. For this transformation, dimethylamine as the key intermediate is generated in situ from dimethylformamide (DMF). All the tested substrates produced the desired products with excellent isolated yields.

Metal-free three-component synthesis of thioamides from β-nitrostyrenes, amines and elemental sulfur

A metal-free C[dbnd]C bond cleavage reaction of β-nitrostyrenes in the presence of elemental sulfur and secondary amines/amides is described. Elemental sulfur serves as both a raw material and an oxidant for C[dbnd]C bond cleavage, and secondary amines or amides are both feasible nitrogen sources. Besides mild reaction condition and simple work-up procedure, the method provided thioamides with good to excellent yields.

-Annulation of Azaoxyallyl Cations and Thiocarbonyls for the Assembly of Thiazolidin-4-ones

A base-promoted, efficient [3 + 2] annulation between azaoxyallyl cations and thiocarbonyls is reported for flexible access to highly functionalized thiazolidin-4-one derivatives in good to excellent yields. An intriguing feature of this method is the met