41182-88-1

Basic information

• Product Name: N-Butylbenzimidoyl chloride
• Synonyms: N-Butylbenzimidoyl chloride
• CAS NO: 41182-88-1
• Molecular Formula: C₁₁H₁₄ClN
• Molecular Weight: 0
• Mol File: 41182-88-1.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Butylbenzimidoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: N-Butylbenzimidoyl chloride(41182-88-1)
• EPA Substance Registry System: N-Butylbenzimidoyl chloride(41182-88-1)

Safety Data

• Hazardous Substances Data: 41182-88-1(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 65-85-0 benzoic acid 
• 7332-00-5 n-butylazide 
• 4460-46-2 3-chloro-3-phenyl-3H-diazirine 
• 29175-11-9 N-Benzoyl-N-n-butylcarbamoylchlorid 
• 2782-40-3 N-butylbenzamide 

Downstream Products

• 1439357-04-6 methyl 1-butyl-7-fluoro-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate 
• 1252580-87-2 allyl N-butylbenzimidate 
• 67796-16-1 2-phenyl-3-n-butylquinazoline-4(3H)-one 
• 10264-08-1 N-cyclohexyl-2-phenyl-acetamide 
• 40999-33-5 N-Butyl-benzimidic acid 2,2,2-trifluoro-1-phenyl-1-trifluoromethyl-ethyl ester 
• 724-92-5 N-cicloesil-α-ossofenilacetamide 
• 134589-68-7 Butyl-[1-phenyl-hept-2-yn-(E)-ylidene]-amine 
• 134589-72-3 Butyl-diphenylprop-2-yn-(E)-ylidene-amine 
• 36638-93-4 1-(N-butyl-benzimidoyl)-5-methyl-1H-pyrazole-3-carboxylic acid methyl ester 
• 1077-18-5 N-benzylidenebutan-1-amine 
• 92-52-4 biphenyl 
• 16766-99-7 α-phenylbenzylidene-n-butylamine 
• 67682-76-2 2-({[(E)-Butylimino]-phenyl-methyl}-ethyl-arsanyl)-phenylamine 

Relevant articles and documents

Novel Conjugated s-Tetrazine Derivatives Bearing a 4H-1,2,4-Triazole Scaffold: Synthesis and Luminescent Properties

A series of new symmetrical s-tetrazine derivatives, coupled via a 1,4-phenylene linkage with a 4H-1,2,4-triazole ring, were obtained. The combination of these two rings in an extensively coupled system has significant potential applications, mainly in op

Parallel copper catalysis: Diastereoselective synthesis of polyfunctionalized azetidin-2-imines

An efficient and diastereoselective synthesis of highly functionalized azetidin-2-imines has been achieved through a parallel catalysis strategy, including a copper-catalyzed azide-alkyne cycloaddition, a copper-catalyzed Csp-Csp2 cr

Palladium-catalyzed cyclocarbonylation of o-lodoanilines with Imidoyl Chlorides to produce quinazolin-4(3H)-ones

A wide variety of substituted quinazolin-4(3H)-ones were prepared in 63-91% yields by the palladium-catalyzed cyclocarbonylation of o-iodoanilines with imidoyl chlorides and carbon monoxide. The reaction is believed to proceed via in situ formation of an amidine, followed by oxidative addition, CO insertion, and intramolecular cyclization to give the substituted quinazolin-4(3H)-ones.