3958-38-1 Usage
Uses
Used in Perfumery and Flavoring Industry:
(E)-1-Cyclononene is used as a key ingredient in the creation of fragrances and flavorings due to its strong, sweet odor. It adds depth and complexity to the scents and tastes of various products, enhancing their overall appeal.
Used in Pharmaceutical Industry:
(E)-1-Cyclononene serves as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and medications that can improve human health.
Used in Polymer Industry:
As a building block for polymer production, (E)-1-Cyclononene is used to create a wide range of polymers with diverse applications, from plastics to coatings and adhesives.
Used as a Solvent in Industrial Applications:
(E)-1-Cyclononene is utilized as a solvent in various industrial processes, providing a means to dissolve and process other substances effectively.
Environmental Considerations:
(E)-1-Cyclononene is a highly flammable substance and a potential environmental hazard. It requires careful handling and proper management to prevent soil and water contamination, ensuring the safety of both people and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 3958-38-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,5 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3958-38:
(6*3)+(5*9)+(4*5)+(3*8)+(2*3)+(1*8)=121
121 % 10 = 1
So 3958-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H16/c1-2-4-6-8-9-7-5-3-1/h1-2H,3-9H2/b2-1+
3958-38-1Relevant academic research and scientific papers
TERMINATION REACTIONS OF C5-C12 CYCLOALKYL RADICALS AND CARBENES
Wojnarovits, Laszlo
, p. 1449 - 1452 (2007/10/02)
Reactions of C5-C12 cycloalkyl radicals and carbenes produced during radiolysis, vacuum-u.v. photolysis, and decomposition of cycloalkanone p-tosylhydrazones were investigated.The disproportionation to combination ratios of radicals are ca. 1 and agree with the ratios of linear secondary radicals.The disproportionation smaller cycloalkyl radicals yields cis-cycloalkenes and cycloalkanes; from C9 and C10 cis- and trans-cycloalkenes and cycloalkanes and from C11 and C12 trans-cycloalkenes and cycloalkanes are produced.Both atoms of H2 given off in the elimination reaction from excited cycloalkane molecules orginate from the same carbon atom and in this process carbenes are formed.Rearrangement of small (C5, C6) and large (C11, C12) cycloalkylcarbenes in the solvent of the given cycloalkane occurs by 1,2-hydrogen migration.C7-C10 carbenes rearrange both by hydrogen atom migration and transannular insertion.
