2384-73-8 Usage
Unsaturated hydrocarbon
It has a triple bond between the third and fourth carbon atoms, which means it has fewer hydrogen atoms than a saturated hydrocarbon with the same number of carbon atoms.
Alkyne
The presence of the triple bond between carbon atoms classifies 1-Hepten-3-yne as an alkyne, which is a type of unsaturated hydrocarbon.
Building block in organic synthesis
1-Hepten-3-yne is commonly used as a starting material or building block in the synthesis of various organic compounds.
Reagent in organic chemistry reactions
It serves as a reagent in various organic chemistry reactions, aiding in the formation of new compounds.
Precursor in the production of functionalized alkyne compounds
1-Hepten-3-yne can act as a precursor, helping to create other alkyne compounds with specific functional groups.
Versatile chemical properties
Its unique structure and reactivity make it valuable in research and pharmaceutical industries for the development of new compounds and drugs.
Participation in various chemical reactions
Due to its alkyne structure, 1-Hepten-3-yne can engage in a range of chemical reactions, making it an important compound in synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2384-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2384-73:
(6*2)+(5*3)+(4*8)+(3*4)+(2*7)+(1*3)=88
88 % 10 = 8
So 2384-73-8 is a valid CAS Registry Number.
2384-73-8Relevant articles and documents
Flash Vacuum Pyrolysis of Stabilised Phosphorus Ylides. Part 1. Preparation of Aliphatic and Therminal Alkynes
Aitken, R. Alan,Atherton, J. Ian
, p. 1281 - 1284 (2007/10/02)
Thermal extrusion of Ph3PO from β-oxoalkylidenetriphenylphosphoranes 4 to give the alkynes 5, which under conventional pyrolysis conditions is restricted to cases in which R1 is an electron withdrawing group, has been successfully achieved for R1=H or alkyl by using FVP.The method allows convenient construction of multigram quantities of the alkynes 5 from alkyl halides 1 and allows convenient construction of multigram quantities of the alkynes 5 from alkyl halides 1 and acid chlorides 3 in three steps with good overall yields.Under the conditions used the ylides with R2 = cyclobutyl also undergo less of ethene to provide convenient access to the vinylalkynes 6.
Zum ambivalenten Verhalten von Allyl- und Propargylradikalen unter Pyrolysebedingungen
Ondruschka, Bernd,Zimmermann, Gerhard
, p. 374 - 375 (2007/10/02)
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