16631-62-2 Usage
Uses
Used in Organic Synthesis:
(E and Z)-3-Ethylidenecyclohexene is used as an intermediate in the organic synthesis industry for the production of various chemical compounds. The unique structures of the E and Z isomers allow them to serve as versatile building blocks in the creation of a wide range of molecules with different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E and Z)-3-Ethylidenecyclohexene is used as a key intermediate in the synthesis of certain pharmaceutical compounds. The distinct shapes of the E and Z isomers can be exploited to design molecules with specific biological activities, potentially leading to the development of new drugs with improved efficacy and selectivity.
Used in Chemical Research:
(E and Z)-3-Ethylidenecyclohexene is also utilized in chemical research as a model compound to study the effects of stereochemistry on reaction mechanisms and outcomes. Understanding how these isomers react differently can provide valuable insights into the fundamental principles of organic chemistry and help guide the design of new synthetic routes and strategies.
Used in Material Science:
In the field of material science, (E and Z)-3-Ethylidenecyclohexene may be employed as a component in the development of novel materials with specific properties. The unique geometries of the E and Z isomers can influence the physical and chemical characteristics of the resulting materials, potentially leading to the creation of advanced materials with applications in various industries, such as electronics, aerospace, and automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 16631-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,3 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16631-62:
(7*1)+(6*6)+(5*6)+(4*3)+(3*1)+(2*6)+(1*2)=102
102 % 10 = 2
So 16631-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-2-8-6-4-3-5-7-8/h2,4,6H,3,5,7H2,1H3/b8-2-
16631-62-2Relevant academic research and scientific papers
Buono, Gerard,Peiffer, Gilbert,Mortreux, Andre,Petit, Francis
, p. 937 - 939 (1980)
The asymmetric codimerization of cyclohexa-1,3-diene with ethylene is catalysed by the Ni(cycloocta-1,5-diene)2-AlEt2Cl-L system where L are chiral aminophosphines; optimization of this catalytic system (-70 degC; L/Ni = 10) gives (+)-(S)-3-vinylcyclohexene with 73.5percent optical purity in 87percent chemical yield when (-)-(R)-N-methyl-N-(1-phenylethylamino)diphenylphosphine is used.
Free radical rearrangement of alkenyl epoxy silanes. Isolation of α-trimethylsilyl aldehydes
Robertson, Jeremy,Burrows, Jeremy N.
, p. 3777 - 3780 (2007/10/02)
The thiyl-radical induced fragmentation of alkenyl epoxy silanes has been found to afford α-trimethylsilyl aldehydes as the immediate products. These may be isolated, rearranged to trimethylsilyl dienol ethers, or converted to 1,3-dienes with high stereoselectivity.
