15402-94-5 Usage
Uses
Used in Pharmaceutical Applications:
(5Z)-5-ethylidene-1-methyl-cycloheptene is used as a precursor in the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. It plays a crucial role in the development of new drugs and medicines.
Used in Agricultural Applications:
In the agricultural industry, (5Z)-5-ethylidene-1-methyl-cycloheptene is utilized as a starting material for the production of agrochemicals, such as pesticides and fertilizers, contributing to enhanced crop protection and yield.
Used in Industrial Applications:
(5Z)-5-ethylidene-1-methyl-cycloheptene serves as a key intermediate in the synthesis of various industrial chemicals, including additives, coatings, and polymers. Its versatility in organic synthesis reactions makes it an essential component in the chemical manufacturing process.
Used in Organic Synthesis:
As a member of the cycloalkene family, (5Z)-5-ethylidene-1-methyl-cycloheptene is widely used as a precursor in organic synthesis reactions. Its unique structure allows for the creation of a diverse range of organic compounds, making it an indispensable tool in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 15402-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,0 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15402-94:
(7*1)+(6*5)+(5*4)+(4*0)+(3*2)+(2*9)+(1*4)=85
85 % 10 = 5
So 15402-94-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-3-10-6-4-5-9(2)7-8-10/h3,5H,4,6-8H2,1-2H3/b10-3-
15402-94-5Relevant academic research and scientific papers
Thermal behaviour of selected C10H16 monoterpenes
Stolle, Achim,Brauns, Claudia,Nuechter, Matthias,Ondruschka, Bernd,Bonrath, Werner,Findeisen, Matthias
, p. 3317 - 3325 (2007/10/03)
The presented work investigates the thermal behaviour of selected monoterpenes under various reactor temperatures and residence times (carrier gas, reactor inserts). In addition to the analysis of the liquid products by capillary GC and GC-MS, chemical derivatisation techniques (Diels-Alder reaction, hydrogenation) were used to identify the liquid-phase products. A thermal conversion of β-pinene (1), myrcene (2) and limonene (4) in a reaction network is presented and the experimental evidence for the formation of pyrolysis products by a biradical pathway is discussed. The reaction network was modified based on the identification of additional C10H 16 terpene isomers. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
