4275-07-4

Basic information

• Product Name: N-BUTYRALDEHYDE-ANILINE [CONDENSATION PRODUCTS OF N-BUTYRALDEHYDE AND ANILINE]
• Synonyms: n-butylidene-benzenamin;N-BUTYRALDEHYDE-ANILINE [CONDENSATION PRODUCTS OF N-BUTYRALDEHYDE AND ANILINE];n-Butyraldehyde-aniline [condensation products of n-Butylraldehyde and aniline];N-BUTYRALDEHYDE-ANILINE [CONDENSATION PRODUCTS OF N-BUTYRALDEHYDE AND ANILINE] 98+%;condensationproductsofn-butyraldehydeandaniline;n-butyraldehyde-aniline;butylidene(phenyl)amine;N-phenylbutan-1-imine
• CAS NO: 4275-07-4
• Molecular Formula: C₁₀H₁₃N
• Molecular Weight: 147.21692
• EINECS: 224-275-3
• Product Categories: Industrial/Fine Chemicals
• Mol File: 4275-07-4.mol
• Article Data: 30

Chemical Properties

• Boiling Point: 229.8°Cat760mmHg
• Flash Point: 84.3°C
• Appearance: /
• Density: 0.87g/cm³
• Vapor Pressure: 0.103mmHg at 25°C
• Refractive Index: 1.492
• CAS DataBase Reference: N-BUTYRALDEHYDE-ANILINE [CONDENSATION PRODUCTS OF N-BUTYRALDEHYDE AND ANILINE](CAS DataBase Reference)
• NIST Chemistry Reference: N-BUTYRALDEHYDE-ANILINE [CONDENSATION PRODUCTS OF N-BUTYRALDEHYDE AND ANILINE](4275-07-4)
• EPA Substance Registry System: N-BUTYRALDEHYDE-ANILINE [CONDENSATION PRODUCTS OF N-BUTYRALDEHYDE AND ANILINE](4275-07-4)

Safety Data

• Hazardous Substances Data: 4275-07-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H13N/c1-2-3-9-11-10-7-5-4-6-8-10/h4-9H,2-3H2,1H3/b11-9+

Upstream product

• 123-72-8 butyraldehyde 
• 62-53-3 aniline 
• 98-95-3 nitrobenzene 
• 2325-27-1 N-phenyltriphenyliminophosphorane 
• 622-37-7 Phenyl azide 
• 71-36-3 butan-1-ol 
• 538-51-2 benzylidene phenylamine 
• 1126-78-9 N-(n-butyl)aniline 
• 109-73-9 N-butylamine 
• 135-19-3 β-naphthol 
• 100-52-7 benzaldehyde 
• 6117-91-5 (E/Z)-2-buten-1-ol 
• 857402-61-0 N-(pinacolboryl)aniline 
• 1227476-15-4 Azobenzene 

Downstream Products

• 24764-97-4 2-bromobutanal 
• 62-53-3 aniline 
• 1126-78-9 N-(n-butyl)aniline 
• 439908-47-1 butylphenylcarbamic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl ester 
• 439908-91-5 3-(R)-(butyl(phenyl)carbamoyloxy)-1-(2-phenoxyethyl)-1-azoniabicyclo[2.2.2]octane bromide 
• 439908-92-6 3-(R)-(butyl(phenyl)carbamoyloxy)-1-(3-thiophen-2-ylpropyl)-1-azoniabicyclo[2.2.2]octane bromide 
• 439908-93-7 3-(R)-(butyl(phenyl)carbamoyloxy)-1-(3-phenylpropyl)-1-azoniabicyclo[2.2.2]octane bromide 
• 439908-87-9 3-(R)-(butyl(phenyl)carbamoyloxy)-1-phenethyl-1-azoniabicyclo[2.2.2]octane bromide 
• 75638-40-3 2-Phenylamino-pentanoic acid; hydrochloride 
• 81942-11-2 ethyl 3-anilinohexanoate 
• 101246-25-7 N-(1-propyl-3-butenyl)aniline 
• 87580-53-8 methyl N-(1-butenyl)-N-phenylcarbamate 
• 3290-24-2 3-ethyl-2-propylquinoline 
• 35331-89-6 1-phenyl-3-ethyl-1-aza-1,3-heptadiene 

Relevant articles and documents

Tandem imine formationviaauto-hydrogen transfer from alcohols to nitro compounds catalyzed by a nanomagnetically recyclable copper catalyst under solvent-free conditions

A direct imination reaction was developed by tandem reaction of alcohols and nitro compounds in the presence of Cu-isatin Schiff base-γ-Fe2O3as a nanomagnetically recyclable catalyst under solvent-free conditions. By this method, various imines were prepared in good to high yields from one-pot reaction of various alcohols (primary aromatic and aliphatic) and nitro compounds (aromatic and aliphatic)viaan auto-hydrogen transfer reaction. Use of an inexpensive and easily reusable catalyst, without requiring any additives or excess amounts of benzyl alcohol as the reaction solvent are the other advantages of this method. This catalytic system has the merits of cost effectiveness, environmental benignity, excellent recyclability and good reproducibility.

Photocatalytic one-pot multidirectional N-alkylation over Pt/D-TiO2/Ti3C2: Ti3C2-based short-range directional charge transmission

Visible-light-induced one-pot, multistep, and chemoselectivity adjustable reactions highlight the economical, sustainable, and green process. Herein, we report Pt nanoparticles dispersed on S and N co-doped titanium dioxide/titanium carbide (MXene) (3%Pt/

Ultrasound-assisted construction of a Z-scheme heterojunction with g-C3N4 nanosheets and flower-like Bi2WO6 microspheres and the photocatalytic activity in the coupling reaction between alcohols and amines under visible light irradiation

Flower-like Bi2WO6 microspheres and bulk g-C3N4 were prepared by the hydrothermal method and high-temperature calcining method, respectively. A new method based on the combination of ultrasonic stripping and mechanical stirring was used to obtain uniform composite x-Bi2WO6/g-C3N4 (x is the Bi2WO6 mass ratio) photocatalysts with a Z-scheme heterojunction. In the reaction of benzyl alcohol and aniline to form imine, the optimal composite, 30percent-Bi2WO6/g-C3N4, showed a conversion rate of 87.6percent, which is much higher than that of pure Bi2WO6 and g-C3N4. Characterization by SEM and TEM showed that the ultrasonically stripped g-C3N4 significantly reduced the radial dimension compared to bulk g-C3N4. A uniformly dispersed photocatalytic material was formed, and it maintained a flower-like microsphere structure. Materials characterized by N2 adsorption–desorption isotherms (BET) showed that the specific surface area of the g-C3N4 nanosheets increased by approximately ten times after ultrasonic stripping. The photostability of the composite was verified by cyclic experiments. Under visible light irradiation, the activation energy of the coupling reaction between benzyl alcohol and aniline was found to be decreased by 29.8 kJ mol?1. A capture experiment was used to verify the active species in the photocatalytic system, with the reaction found to be mainly completed through the synergistic action of h+, e? and ?O2?.