6282-00-4

Basic information

• Product Name: N,N-DI-N-PROPYLFORMAMIDE
• Synonyms: N,N-DIPROPYLFORMAMIDE;N,N-DI-N-PROPYLFORMAMIDE;TIMTEC-BB SBB008026;Dipropylformamide;Formamide, N,N-di-n-propyl-;Formamide, N,N-dipropyl-;n,n-di-n-propyl-formamid;N,N-Di-n-propylformamide,96%
• CAS NO: 6282-00-4
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2
• Mol File: 6282-00-4.mol
• Article Data: 36

Chemical Properties

• Boiling Point: 100-101°C 18mm
• Flash Point: 88°C
• Appearance: yellowish gray liquid
• Density: 0.889 g/cm3 (20℃)
• Vapor Pressure: 0.108mmHg at 25°C
• Refractive Index: 1.4395
• Storage Temp.: Sealed in dry,Room Temperature
• BRN: 635928
• CAS DataBase Reference: N,N-DI-N-PROPYLFORMAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DI-N-PROPYLFORMAMIDE(6282-00-4)
• EPA Substance Registry System: N,N-DI-N-PROPYLFORMAMIDE(6282-00-4)

Safety Data

• Statements: 36/38
• Safety Statements: 26-36
• RTECS: LQ2625000
• Hazardous Substances Data: 6282-00-4(Hazardous Substances Data)

Usage

Definition

ChEBI: A formamide in which the amide hydrogens of formamide are replaced by propyl groups.

InChI:InChI=1/C7H15NO/c1-3-5-8(7-9)6-4-2/h7H,3-6H2,1-2H3

Upstream product

• 70785-80-7 dipropyl-oxalamic acid 
• 64-18-6 formic acid 
• 142-84-7 di-n-propylamine 
• 201230-82-2 carbon monoxide 
• 108-03-2 1-Nitropropane 
• 141-53-7 sodium formate 
• 124-38-9 carbon dioxide 
• 122-51-0 orthoformic acid triethyl ester 
• 66772-82-5 N,N-di-n-propyl-1-imidazolecarboxamide 
• 113388-44-6 (formyloxy)(acetoxy)phenylmethane 
• 102-69-2 tri-n-propylamine 
• 96-26-4 dihydroxyacetone 
• 109-94-4 formic acid ethyl ester 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1238675-78-9 N,N-dipropyl-(diphenylphosphinomethylene)iminium iodide 
• 3405-42-3 N-methyldipropylamine 
• 14657-86-4 N,N-dipropylbenzamide 
• 54408-44-5 S-Phenyl N,N-dipropylthiocarbamate 
• 17364-40-8 4,5-dihydro-1,3-diphenyl-5-oxo-1H-pyrazole-4-carboxaldehyde 

Relevant articles and documents

Mesoporous Sn(IV) Doping DFNS Supported BaMnO3 Nanoparticles for Formylation of Amines Using Carbon Dioxide

Abstract: In the present paper, Sn(IV) doping DFNS (SnD) supported nanoparticles of BaMnO3 (BaMnO3/SnD) and using as a catalyst for the N-formylation of amines by CO2 hydrogenation. In this catalyst, the SnD with the ratios of Si/Sn in the range of from 6 to 50 were obtained with method of direct hydrothermal synthesis (DHS) as well as the nanoparticles of BaMnO3 were on the surfaces of SnD in situ reduced. Scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), X-ray energy dispersive spectroscopy (EDS), and transmission electron microscopy (TEM) were utilized for characterizing the nanostructures BaMnO3/SnD. It is found that the nanostructures of BaMnO3/SnD can be a nominate due to its effective and novel catalytic behavior in N-formylation of amines through hydrogenation of CO2. Graphic Abstract: [Figure not available: see fulltext.]

The synthesis of cyanoformamides via a CsF-promoted decyanation/oxidation cascade of 2-dialkylamino-malononitriles

A mild and efficient method for the synthesis of cyanoformamides from N,N-disubstituted aminomalononitriles with CsF as the promoter has been developed. This method features a wide substrate scope and high reaction efficiency, and will facilitate corresponding cyanoformamide-based biological studies and synthetic methodology development.

Method for preparing N-formylated amine compounds

The invention discloses a method for preparation N-formylated amine compounds. In the method, the amine compounds and 1,3-dihydroxy acetone are taken as reaction raw materials reacting in a reactor for 2-48 hours at the reaction temperature of 0-100DEG C in a reaction medium in the presence of composite catalysts and oxidants, and the N-formylated amine compounds are obtained. The method is simpleand moderate in reaction conditions, cost can be reduced, target products can be obtained with high yield, and the catalysts used have high catalytic activity and are easy to be separated from a reaction system and reuses; the method is environment friendly during the whole process, the reaction raw materials are easy to be converted from biodiesel by-product propylene glycol, and use of glycerolis facilitated.