1609007-77-3

Basic information

• Product Name: methyl 3-[(4-cyanobenzoyl)-N-ethylamino]-2-methoxybenzoate
• Synonyms: methyl 3-[(4-cyanobenzoyl)-N-ethylamino]-2-methoxybenzoate
• CAS NO: 1609007-77-3
• Molecular Weight: 338.363
• Mol File: 1609007-77-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 3-[(4-cyanobenzoyl)-N-ethylamino]-2-methoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-[(4-cyanobenzoyl)-N-ethylamino]-2-methoxybenzoate(1609007-77-3)
• EPA Substance Registry System: methyl 3-[(4-cyanobenzoyl)-N-ethylamino]-2-methoxybenzoate(1609007-77-3)

Safety Data

• Hazardous Substances Data: 1609007-77-3(Hazardous Substances Data)

Upstream product

• 5129-25-9 2-methoxy-3-methoxycarbonylaniline 
• 74-96-4 ethyl bromide 
• 1609007-78-4 methyl 3-[(4-cyanobenzoyl)amino]-2-methoxybenzoate 
• 6068-72-0 4-cyanobenzoyl chlorIde 
• 90564-26-4 2-methoxy-3-nitro-benzoic acid methyl ester 
• 1609007-76-2 methyl 3-(ethylamino)-2-methoxybenzoate 

Downstream Products

• 1609007-79-5 3-[(4-cyanobenzoyl)-N-ethylamino]-2-methoxybenzoic acid 
• 1609007-65-9 N-[2-bromo-6-chloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-3-[(4-cyanobenzoyl)ethylamino]-2-methoxybenzamide 
• 1609007-80-8 3-[(4-cyanobenzoyl)ethylamino]-2-methoxybenzoyl chloride 

Relevant articles and documents

INSECTICIDAL COMPOUNDS

The present invention relates to novel triazole derivatives of formula (I) having insecticidal activity, to processes and intermediates for preparing them, to insecticidal, acaricidal, nematicidal or molluscicidal compositions comprising them and to methods of using them to combat and control insect, acarine, nematode or mollusc pests wherein R1, R2, G1, G2, Q1 and Q2 are as defined in claim 1; or salts thereof.

PROCESS FOR THE PREPARATION OF AMIDES FROM HINDERED ANILINES CONTAINING A PERHALOALKYL GROUP

The present invention provides a novel and improved process for the production of the production of hindered anilines containing perfluoroalky groups in good yield any by using close to stoichiometric amounts of acylating agent.