153172-71-5

Basic information

• Product Name: N-(2-cyanophenyl)-4-methoxybenzamide
• Synonyms: N-(2-cyanophenyl)-4-methoxybenzamide
• CAS NO: 153172-71-5
• Molecular Formula: C₁₅H₁₂N₂O₂
• Molecular Weight: 252.27
• Mol File: 153172-71-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-cyanophenyl)-4-methoxybenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-cyanophenyl)-4-methoxybenzamide(153172-71-5)
• EPA Substance Registry System: N-(2-cyanophenyl)-4-methoxybenzamide(153172-71-5)

Safety Data

• Hazardous Substances Data: 153172-71-5(Hazardous Substances Data)

Upstream product

• 873-32-5 2-Chlorobenzonitrile 
• 3424-93-9 4-methoxyphenylacetamide 
• 1885-29-6 anthranilic acid nitrile 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 5784-95-2 2-(4-methoxyphenyl)-1H-indole 
• 24310-46-1 4-methoxyacetophenone phenylhydrazone 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 13939-06-5 molybdenum hexacarbonyl 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 84570-80-9 2-(4-methoxylphenyl)-4-phenylquinazoline 

Relevant articles and documents

Nickel-Catalyzed N -Arylation of Amides with (Hetero)aryl Electrophiles by Using a DBU/NaTFA Dual-Base System

The first nickel-catalyzed N -arylation of amides with (hetero)aryl (pseudo)halides employing an organic amine base is described. By using a bis(cyclooctadienyl)nickel/8-[2-(dicyclohexylphosphinyl)phenyl]-1,3,5,7-tetramethyl-2,4,6-trioxa-8-phosphaadamantane catalyst mixture in combination with DBU/NaTFA as a dual-base system, a diversity of (hetero)aryl chloride, bromide, tosylate, and mesylate electrophiles were successfully cross-coupled with structurally diverse primary amides, as well as a selection of secondary amide, lactam, and oxazolidone nucleophiles.

Pd-Catalyzed tandem reaction of N-(2-cyanoaryl)benzamides with arylboronic acids: synthesis of quinazolines

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Synthesis of 2-Aminobenzonitriles through Nitrosation Reaction and Sequential Iron(III)-Catalyzed C-C Bond Cleavage of 2-Arylindoles

A variety of 2-aminobenzonitriles were prepared from 2-arylindoles in good to excellent yields through tert-butylnitrite (TBN)-mediated nitrosation and sequential iron(III)-catalyzed C-C Bond cleavage in a one-pot fashion. The 2-aminobenzonitriles can be used to rapidly synthesize benzoxazinones by intramolecular condensation. The present method features an inexpensive iron(III) catalyst, gram scalable preparations, and novel C-C bond cleavage of indoles.

SAR Studies of N-[2-(1 H-Tetrazol-5-yl)phenyl]benzamide Derivatives as Potent G Protein-Coupled Receptor-35 Agonists

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Structure activity relationships, multidrug resistance reversal and selectivity of heteroarylphenyl ABCG2 inhibitors

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Palladium-catalyzed carbonylative synthesis of N-(2-cyanoaryl)benzamides and sequential synthesis of quinazolinones

A convenient procedure for the synthesis of N-(2-cyanoaryl)benzamides has been developed. Using aryl bromides and 2-aminobenzonitriles as the substrates, Mo(CO)6 as the CO source, the desired amides were produced in good yields. Quinazolinones

Synthesis of quinazolinone analogues using sodium perborate as catalyst

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Anchimeric Assistance in the Specific Acid-catalyzed Hydration of Benzonitriles

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