6043-42-1

Basic information

• Product Name: Benzamide, 3,4-dichloro-N-phenyl-
• CAS NO: 6043-42-1
• Molecular Formula: C13H9Cl2NO
• Molecular Weight: 266.127
• Mol File: 6043-42-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzamide, 3,4-dichloro-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 3,4-dichloro-N-phenyl-(6043-42-1)
• EPA Substance Registry System: Benzamide, 3,4-dichloro-N-phenyl-(6043-42-1)

Safety Data

• Hazardous Substances Data: 6043-42-1(Hazardous Substances Data)

Upstream product

• 694-59-7 pyridine N-oxide 
• 87282-01-7 3,4-Dichloro-N-phenyl-benzimidoyl chloride 
• 62-53-3 aniline 
• 3024-72-4 3,4-dichlorobenzoyl chloride 
• 6582-42-9 1-(3,4-dichlorophenyl)propan-1-one 
• 51-44-5 3,4-dichlorbenzoic acid 

Downstream Products

• 89564-67-0 4-(3,4-Dichloro-benzoylamino)-benzenesulfonyl chloride 
• 89565-05-9 C₂₀H₁₅Cl₃N₄O₄S 
• 89564-97-6 C₂₀H₁₄Cl₂N₄O₅S 
• 89564-96-5 C₂₁H₁₇Cl₂N₃O₄S 
• 89565-03-7 C₁₆H₁₅Cl₂N₃O₅S 
• 89564-95-4 C₂₁H₁₇Cl₂N₃O₃S 
• 89564-94-3 C₂₀H₁₅Cl₂N₃O₃S 
• 89564-99-8 3,4-Dichloro-N-[4-(3,5-dimethyl-pyrazole-1-sulfonyl)-phenyl]-benzamide 
• 89564-98-7 C₁₉H₁₉Cl₂N₃O₃S 
• 89565-02-6 N-(4-Benzylsulfamoyl-phenyl)-3,4-dichloro-benzamide 
• 89565-01-5 3,4-Dichloro-N-(4-phenylsulfamoyl-phenyl)-benzamide 
• 89565-04-8 C₁₅H₁₅Cl₂N₃O₃S 
• 89564-93-2 C₁₆H₁₅Cl₂N₃O₃S 
• 89565-00-4 3,4-Dichloro-N-(4-dimethylsulfamoyl-phenyl)-benzamide 

Relevant articles and documents

Copper-catalyzed aerobic oxidative C-C bond cleavage of simple ketones for the synthesis of amides

A Cu-catalyzed oxidative amidation of simple ketones with amines via carbon-carbon (C-C) bond cleavage has been developed. A number of aryl and alkyl ketones could be easily converted to amides using cheap copper salt as the catalyst and O2 as the oxidant with a wide range of amines, including primary and secondary amines. This method shows a notable advantage of the broad scope for the substrate, thus providing a practical approach to amides. A plausible mechanism is proposed based on the preliminary experiments.

Selective antagonists of mouse trace amine-associated receptor 1 (mTAAR1): Discovery of EPPTB (RO5212773)

High throughput screening of the Roche compound library identified benzanilides such as 1 and 2 as antagonists of TAAR1. Optimisation of this hit series led to the first selective TAAR1 antagonist (N-(3-Ethoxy-phenyl)-4- pyrrolidin-1-yl-3-trifluoromethyl-

Direct Acylamination of Pyridine 1-Oxide with N-Phenylarenimidoyl Chlorides and Fluorides

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