5922-69-0 Usage
Description
N-[3-(dimethylamino)propyl]formamide is a formamide derivative with a molecular formula of C6H14N2O. It features a dimethylamino group attached to a propyl chain, resulting in a colorless to pale yellow liquid with a faint amine odor. N-[3-(dimethylamino)propyl]formamide is soluble in water, alcohols, and most organic solvents, making it versatile for various applications.
Uses
Used in Pharmaceutical Production:
N-[3-(dimethylamino)propyl]formamide serves as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new medications.
Used in Agrochemical Production:
N-[3-(dimethylamino)propyl]formamide is also utilized as an intermediate in the production of agrochemicals, aiding in the creation of products for agricultural applications.
Used in Chemical Synthesis:
N-[3-(dimethylamino)propyl]formamide acts as a reagent in chemical synthesis reactions, specifically for introducing the dimethylamino group into organic molecules.
Used as a Solvent:
Due to its solubility properties, this compound has been studied for potential use as a solvent in various chemical processes.
Used as a Corrosion Inhibitor:
N-[3-(dimethylamino)propyl]formamide has been explored for its potential as a corrosion inhibitor, offering protection against the deterioration of materials in certain industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5922-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5922-69:
(6*5)+(5*9)+(4*2)+(3*2)+(2*6)+(1*9)=110
110 % 10 = 0
So 5922-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O/c1-8(2)5-3-4-7-6-9/h6H,3-5H2,1-2H3,(H,7,9)
5922-69-0Relevant articles and documents
ZWITTERIONIC COMPOUNDS AND USE THEREOF
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Page/Page column 5, (2009/04/24)
The present invention covers zwitterionic, non-surface-active compounds in the form of carboxymethylated, short-chain dialkylaminoalkylamides and use thereof as therapeutic agent.
Long-range anisotropic effects of long chain amides
Budzikiewicz, Herbert,Vieth, Peter-Eric,Krueger, Uwe
, p. 825 - 840 (2007/10/02)
In 1H-NMR spectra of amids with long-chain aliphatic N-substituents one observes - despite of the free mobility of the aliphatic chain - splitting of the signals of the terminal methyl groups which is caused by the hindered rotation of the amide bond. - Keywords: Amides; Hindered rotation; 1H-NMR
