6710-72-1

Basic information

• Product Name: ACET-D3-ANILIDE
• Synonyms: ACET-D3-ANILIDE
• CAS NO: 6710-72-1
• Molecular Formula: C₈H₉NO
• Molecular Weight: 138.18
• Mol File: 6710-72-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ACET-D3-ANILIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ACET-D3-ANILIDE(6710-72-1)
• EPA Substance Registry System: ACET-D3-ANILIDE(6710-72-1)

Safety Data

• Hazardous Substances Data: 6710-72-1(Hazardous Substances Data)

Upstream product

• 2206-26-0 [D₃]acetonitrile 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 62-53-3 aniline 
• 19259-90-6 [2H₃]acetyl chloride 
• 831-91-4 Benzyl phenyl sulfide 

Downstream Products

• 86099-77-6 N-(<2,2,2-d3>ethyl)aniline 
• 86099-80-1 2-cyclohexanone 

Relevant articles and documents

Direct synthesis of N-arylamides via the coupling of aryl diazonium tetrafluoroborates and nitriles under transition-metal-free conditions

The direct synthesis of N-arylamides via the coupling of aryl diazonium tetrafluoroborates and nitriles under transition-metal-free conditions has been developed. The reported protocol is practical and represents an efficient method to produce functionalized amides in moderate to good yields.

DEUTERATED N-ETHYL-N-PHENYL-1,2-DIHYDRO-4-HYDROXY-5-CHLORO-1-METHYL-2-OXOQUINOLINE-3-CARBOXAMIDE, SALTS AND USES THEREOF

The subject invention provides deuterated N-ethyl-N-phenyl-1,2-dihydro-4-hydroxy-5-chloro-1-methyl-2-oxoquinoline-3-carboxamide, its salts and uses.

Photoinduced electron transfer reactions of benzyl phenyl sulfides promoted by 9,10-dicyanoanthracene

The photoinduced oxidation of benzyl phenyl sulfides 1-3 has been investigated in MeCN using 9,10-dicyanoanthracene as sensitizer in the presence of O2. In this reaction a sulfide radical cation is formed, which undergoes one or more of the three main reaction pathways opened to these species: C-S bond cleavage, C-H bond cleavage and S-oxidation. The former route (leading to benzylic products) was observed with all the substrates investigated, whereas the second (leading to benzaldehydes) operates only with 1 and 2. Formation of sulfoxides was found solely in the photooxidation of 1. The influence of substrate structures on the relative contribution of the three pathways as well as the role of O2- in this respect are discussed.