17699-86-4 Usage
Physical state
Colorless liquid
1-methyl-4-vinyl-1-cyclohexene is a liquid that is colorless in appearance.
Odor
Pungent
This compound has a strong, pungent odor that can be detected easily.
Usage in polymer and resin production
Commonly used
1-methyl-4-vinyl-1-cyclohexene is frequently used as a key ingredient in the creation of polymers and resins.
Monomer in synthesis
Other chemicals
As a monomer, 1-methyl-4-vinyl-1-cyclohexene is used as a building block for synthesizing various other chemicals, such as plasticizers, adhesives, and coatings.
Importance in fragrance and flavor manufacturing
Intermediate
This compound plays a significant role as an intermediate in the production of fragrances and flavors.
Versatility and reactivity
Valuable in the chemical industry
Due to its ability to react and be used in a wide range of applications, 1-methyl-4-vinyl-1-cyclohexene is considered a valuable compound in the chemical industry, contributing to the creation of numerous products.
Check Digit Verification of cas no
The CAS Registry Mumber 17699-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,9 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17699-86:
(7*1)+(6*7)+(5*6)+(4*9)+(3*9)+(2*8)+(1*6)=164
164 % 10 = 4
So 17699-86-4 is a valid CAS Registry Number.
17699-86-4Relevant articles and documents
Cross-Dehydrocycloaddition of 1,3-Butadien with Isoprene over MgO and ZrO2
Suzuka, Hiroyasu,Hattori, Hideshi
, p. 1332 - 1335 (2007/10/02)
A mixture comprising of equal amounts of 1,3-butadiene (BD) and isoprene(IPN) was allowed to react over MgO and ZrO2 at 473 K in order to examine the relation between the product distribution and the reaction mechanisms.Over ZrO2 the most abundant product was 4-ethyltoluene, which was produced by a base-catalyzed Diels-Alder reaction between BD and IPN, followed by double-bond migration and dehydrogenation.In the Diels-Alder reaction, IPN acts as a diene and BD acts as a dienophile.Over MgO, o-xylene was primarily produced by anionic mechanisms.Among the products formed from BD and IPN, 4-ethyltoluene was produced most, though the production of 3-ethyltoluene was considerable.The active sites on ZrO2 were strongly poisoned by both CO2 and NH3.The active sites on MgO were completely poisoned by CO2, and were modified by NH3 in such a way that the reaction mechanisms changed from the anionic mechanisms to those involving Diels-Alder reaction.
