7138-58-1

Basic information

• Product Name: Benzenamine, N-propylidene-
• CAS NO: 7138-58-1
• Molecular Formula: C9H11N
• Molecular Weight: 133.193
• Mol File: 7138-58-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-propylidene-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-propylidene-(7138-58-1)
• EPA Substance Registry System: Benzenamine, N-propylidene-(7138-58-1)

Safety Data

• Hazardous Substances Data: 7138-58-1(Hazardous Substances Data)

Upstream product

• 71-23-8 propan-1-ol 
• 98-95-3 nitrobenzene 
• 123-38-6 propionaldehyde 
• 62-53-3 aniline 
• 589-09-3 N-allyl-N-phenylamine 
• 31144-24-8 N-Phenylpropionimidoyl chloride 
• 620-71-3 N-(phenyl)-2-methylacetamide 

Downstream Products

• 88091-04-7 2,5-Dimethyl-1-phenyl-1H-pyridin-4-one 
• 622-80-0 N-propylaniline 
• 67467-96-3 2-methyl-3-(4-(tert-pentyl)phenyl)propanal 
• 55240-30-7 N-n-propyl-N-phenyl carbamoyl chloride 
• 1312718-55-0 C₁₇H₂₄N₂O₂ 
• 124687-82-7 Phenyl-[(S)-1-((R)-toluene-4-sulfinylmethyl)-propyl]-amine 
• 124687-83-8 Phenyl-[(R)-1-((R)-toluene-4-sulfinylmethyl)-propyl]-amine 
• 124687-84-9 [(S)-1-((R)-Benzenesulfinylmethyl)-propyl]-phenyl-amine 
• 124687-92-9 [(R)-1-((R)-Benzenesulfinylmethyl)-propyl]-phenyl-amine 

Relevant articles and documents

Kinetic and equilibrium studies of anilinoalkanesulfonate formation

1H NMR studies of the reactions of some hydroxyalkanesulfonates, 1, with aniline derivatives, 2, show the formation at equilibrium of anilinoalkanesulfonates, 3. Kinetic studies in water are consistent with a mechanism involving dissociation of

NCP ligand, [...] complex, synthesis method, intermediate and application

The invention discloses an NCP ligand, iridium complex, synthetic method, intermediate and application thereof. The invention provides an NCP ligand and an NCP ligand iridium complex, wherein R1, R2, R3, R4, R5, R6 and R7 separately represent hydrogen atom or C1-C30 alkyl, R' and R'' independently represent C1-C30 alkyl. The invention provides the application of the NCP ligand iridium complex to the catalysis of alkane dehydrogenation reaction, olefin isomerization reaction, alcohol dehydrogenation reaction, ester alpha alkylation reaction, and amide alpha alkylation reaction. The NCP ligand provided by the invention contains dialkyl substituted phosphine, which has strong electron donating ability and can form a NCP ligand iridium complex by complexing with iridium. The NCP ligand iridium complex uses pyridine to replace a conventional alkyl phosphate electron donor, and has the advantages of good stability, high selectivity on alkane dehydrogenation reaction, mild reaction conditions, good catalytic effect, and industrial production prospect.

METHOD FOR THE CATALYTIC REDUCTION OF ACID CHLORIDES AND IMIDOYL CHLORIDES

The present application relates to methods for the catalytic reduction of acid chlorides and/or imidoyl chlorides. The methods comprise reacting the acid chloride or imidoyl chloride with a silane reducing agent in the presence of a catalyst such as [Cp(Pri3P)Ru(NCMe)2]+[PF6]?.