37771-22-5

Basic information

• Product Name: Benzenecarboximidoyl chloride, 4-methoxy-N-(4-methoxyphenyl)-
• CAS NO: 37771-22-5
• Molecular Formula: C15H14ClNO2
• Molecular Weight: 275.735
• Mol File: 37771-22-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidoyl chloride, 4-methoxy-N-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidoyl chloride, 4-methoxy-N-(4-methoxyphenyl)-(37771-22-5)
• EPA Substance Registry System: Benzenecarboximidoyl chloride, 4-methoxy-N-(4-methoxyphenyl)-(37771-22-5)

Safety Data

• Hazardous Substances Data: 37771-22-5(Hazardous Substances Data)

Upstream product

• 100-07-2 4-methoxy-benzoyl chloride 
• 104-94-9 4-methoxy-aniline 
• 27865-44-7 4-methoxy-N-(4-methoxyphenyl)benzamide 

Downstream Products

• 84425-51-4 2-(4-Methoxy-phenyl)-5,7-diphenyl-[1,3,4]thiadiazolo[3,2-a]pyridin-4-ylium; chloride 
• 104-94-9 4-methoxy-aniline 
• 82020-07-3 bis (methoxy-4 phenyl)-3,4 ethyl-5 4H-triazole-1,2,4 
• 21202-70-0 6-methoxy-2-(4-methoxy-phenyl)-quinolin-4-ol 
• 101971-78-2 Acetic acid 4-[3-(4-acetoxy-phenyl)-5-ethyl-[1,2,4]triazol-4-yl]-phenyl ester 
• 82020-39-1 4,4'-(3-ethyl-4H-1,2,4-triazol-4,5-diyl)-bis-phenol 

Relevant articles and documents

Domino 1,4- And 1,6-Addition Reactions of Ketene Silyl Acetals to Dialkynyl Imines Promoted by Aluminum Chloride: Synthesis of Multifunctionalized β-Lactams

Domino 1,4- and 1,6-addition reactions of ketene silyl acetals to dialkynyl imines are disclosed. Aluminum chloride promoted domino 1,4- and 1,6-addition reactions of ketene silyl acetals to dialkynyl imines to give a variety of alkenyl iminocyclobutenones in moderate to good yields. The chemoselective reduction of alkenyl iminocyclobutenones and the subsequent thermal rearrangement of resulting alkenyl aminocyclobutenones in the presence of appropriate amines provided cis or trans multifunctionalized β-lactams in moderate to high yields with good to high diastereoselectivities.

Umpolung of Michael acceptors catalyzed by N-heterocyclic carbenes

N-Heterocyclic carbenes can catalyze β-alkylations of a range of α,β-unsaturated esters, amides, and nitriles that bear pendant leaving groups to form a variety of ring sizes. In this process, the nucleophilic catalyst transiently transforms the normally electrophilic β carbon into a nucleophilic site through an unanticipated addition-tautomerization sequence. Copyright

TETRAZOLES. XXVIII PREPARATION AND PROPERTIES OF 2,3-DIPHENYL-5-ALKYLTETRAZOLIUM SALTS

The oxidation of 1,5-diphenyl-3-alkylformazanes by potassium permanganate in methylene chloride (chloroform)-water two-phase systems is a convenient method for the preparation of 2,3-diphenyl-5-alkyltetrazolium salts.The 2,3-diphenyl-5-alkyltetrazolium salts can be used as catalysts for interphase transfer in reactions proceeding in organic solvent-water two-phase systems, with a neutral or acid aqueous phase.The catalytic activity of 2,3-diphenyl-5-alkyltetrazolium salts increases with increase in the length of the alkyl substituent in the 5-position of the tetrazole ring.