30438-94-9

Basic information

• Product Name: N,N-diallyl-4-chloroaniline
• Synonyms: N,N-diallyl-4-chloroaniline
• CAS NO: 30438-94-9
• Molecular Formula: C₁₂H₁₄ClN
• Molecular Weight: 207.69926
• Mol File: 30438-94-9.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N,N-diallyl-4-chloroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diallyl-4-chloroaniline(30438-94-9)
• EPA Substance Registry System: N,N-diallyl-4-chloroaniline(30438-94-9)

Safety Data

• Hazardous Substances Data: 30438-94-9(Hazardous Substances Data)

Upstream product

• 106-47-8 4-chloro-aniline 
• 106-95-6 allyl bromide 
• 1121-60-4 pyridine-2-carbaldehyde 
• 15022-08-9 diallylcarbonate 
• 3296-05-7 1-azido-4-chlorobenzene 
• 107-18-6 allyl alcohol 

Downstream Products

• 5044-38-2 1-(4-chlorophenyl)-1H-pyrrole 
• 28192-10-1 1-(4-chlorophenyl)-2,5-dihydro-1H-pyrrole 
• 1316312-70-5 ethyl allyl-(2-allyl-4-chloro-phenyl)carbamate 
• 1316312-41-0 6-chloro-2-methyl-1-(toluene-4-sulfonyl)-1,2-dihydro-quinoline 
• 1316312-33-0 ethyl 6-chloro-2-methyl-2H-quinoline-1-carboxylate 
• 1316312-22-7 N-(2-buta-1,3-dienyl-4-chloro-phenyl)-2,2,2-trifluoro-acetamide 
• 1316312-21-6 N-(2-buta-1,3-dienyl-4-chloro-phenyl)-acetamide 
• 1316312-20-5 N-(2-buta-1,3-dienyl-4-chloro-phenyl)-benzamide 
• 1316312-19-2 N-(2-buta-1,3-dienyl-4-chlorophenyl)-4-methyl-benzenesulfonamide 
• 1316312-03-4 ethyl (2-buta-1,3-dienyl-4-chlorophenyl)carbamate 
• 1316312-75-0 N-allyl-N-(2-allyl-4-chlorophenyl)-2,2,2-trifluoroacetamide 
• 1316312-74-9 N-allyl-N-(2-allyl-4-chlorophenyl)acetamide 
• 1118507-67-7 C₁₇H₁₄ClNO 
• 1118507-61-1 C₁₇H₁₆ClNO₂S 

Relevant articles and documents

Highly efficient Ru(ii)-alkylidene based Hoveyda-Grubbs catalysts for ring-closing metathesis reactions

Three novel phosphine-free Ru-alkylidenes (7a-7c) have been synthesized and utilized as efficient catalysts for ring closing metathesis (RCM) reaction. Spectroscopic data, i.e. NMR and HRMS, along with single crystal X-ray diffraction analysis, were used

Assisted tandem catalytic RCM-aromatization in the synthesis of pyrroles and furans

An assisted tandem catalytic transformation of diallyl amines and diallyl ethers into N-aryl pyrroles and furans, respectively, is described. The sequence relies on ring closing metathesis followed by dehydrogenation of the initially formed dihydropyrroles and dihydrofurans. Both steps are Ru-catalyzed, but the sequence requires only one precatalyst, because conversion of the metathesis catalyst into the dehydrogenation catalyst is achieved in situ, triggered by the oxidant tert-butyl hydroperoxide.

Palladium-catalyzed cyclization/cyclopropanation reaction for the synthesis of fused N-containing heterocycles

Palladium-catalyzed cyclization/cyclopropanation can be used to convert a range of substituted cyclic N-aryl allyl/methallyl amines efficiently and selectively to the corresponding fused tetrahydropyridine/cyclopropane-fused isoquinoline derivatives via β