61958-17-6 Usage
Description
(E)-3-chloro-2-ethylbut-2-enal, also known as 3-chloro-2-ethyl-2-butenal, is a chemical compound with the formula C6H9ClO. It is a colorless to pale yellow liquid with a pungent odor and is classified as an aldehyde, containing a carbonyl group (C=O) bonded to a hydrogen and a carbon atom. (E)-3-chloro-2-ethylbut-2-enal is also used as an intermediate in the synthesis of other organic compounds and can be found in some natural sources such as certain plants and marine organisms. Due to its flammability and potential to cause skin and eye irritation, it is important to handle (E)-3-chloro-2-ethylbut-2-enal with caution.
Uses
Used in Pharmaceutical Industry:
(E)-3-chloro-2-ethylbut-2-enal is used as a key compound in the production of pharmaceuticals, contributing to the development of various medications due to its unique chemical properties.
Used in Fragrance Industry:
(E)-3-chloro-2-ethylbut-2-enal is also utilized as a component in the creation of fragrances, where its distinct odor can be manipulated to produce a wide range of scents for different applications.
Used in Flavoring Industry:
(E)-3-chloro-2-ethylbut-2-enal is employed in the flavoring industry to enhance the taste of various food products, taking advantage of its pungent and distinctive flavor profile.
Used as an Intermediate in Organic Synthesis:
In addition to its direct applications, (E)-3-chloro-2-ethylbut-2-enal serves as an intermediate in the synthesis of other organic compounds, further expanding its utility in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 61958-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,5 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61958-17:
(7*6)+(6*1)+(5*9)+(4*5)+(3*8)+(2*1)+(1*7)=146
146 % 10 = 6
So 61958-17-6 is a valid CAS Registry Number.
61958-17-6Relevant articles and documents
Configurational Regidity and Reduced 1H NMR Shifts of Some (Pseudo)tetrahedral Nickel(II) Bis-chelates of 1,3-Diimines
Knorr, Rudolf,Weiss, Alfons
, p. 2104 - 2115 (2007/10/02)
The twofold condensation of 1,3-dioxo compounds with alkylamines affods 1,3-diimines.Two 3-oxoenamines 10 analogously prepared from aniline are converted to quinolines 12 when a second condensation is attempted. 1H NMR spectra of the paramagnetic, fully t
