6537-04-8 Usage
Molecular structure
1-(bicyclo[4.1.0]hept-7-yl)ethyl ethyl ether is an ether derivative with a complex molecular structure, consisting of a bicyclic ring system containing seven carbon atoms and an ethyl group.
Functional groups
The compound contains an ether functional group (R-O-R') and an ethyl group (C2H5).
Bicyclic ring system
The compound features a bicyclic ring system with seven carbon atoms, specifically a bicyclo[4.1.0]heptane ring.
Solvent properties
1-(bicyclo[4.1.0]hept-7-yl)ethyl ethyl ether is often used as a solvent in various chemical processes due to its ability to dissolve a wide range of substances.
Intermediate in chemical syntheses
The compound serves as an intermediate in the synthesis of other chemicals, making it a valuable building block in the chemical industry.
Applications
1-(bicyclo[4.1.0]hept-7-yl)ethyl ethyl ether finds use in a range of applications, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Safety precautions
Due to its complex nature, caution should be exercised when handling and using 1-(bicyclo[4.1.0]hept-7-yl)ethyl ethyl ether to ensure safety and proper handling.
Stability
The compound may have specific stability requirements, such as storage conditions or compatibility with other substances, to maintain its integrity and performance.
Reactivity
1-(bicyclo[4.1.0]hept-7-yl)ethyl ethyl ether may exhibit reactivity with certain chemicals, requiring careful consideration when used in chemical reactions or syntheses.
Purity
The purity of 1-(bicyclo[4.1.0]hept-7-yl)ethyl ethyl ether can impact its performance and safety, making it essential to ensure high-quality, pure samples for use in chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 6537-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6537-04:
(6*6)+(5*5)+(4*3)+(3*7)+(2*0)+(1*4)=98
98 % 10 = 8
So 6537-04-8 is a valid CAS Registry Number.
6537-04-8Relevant academic research and scientific papers
REACTIONS OF gem-DIBROMOCYCLOALKANES WITH METHYLLITHIUM
Molchanov, A. P.,Kalyamin, S. A.,Kostikov, R. R.
, p. 102 - 107 (2007/10/02)
In the reaction of 7,7-dibromonorcarane with methyllithium tricyclo2,7>heptane, 7-(1-ethoxyethyl)bicycloheptane, and 7,7-bisnorcaranylidene are formed, and the proportions of these depnd on the reaction temperature.Substituted gem-dibromobicycloheptanes react analogously. 6,6-Dibromobicyclohexanes substituted in the 1 position react with methyllithium with the formation of 3,12-disubstituted tricyclo2,7>dodeca-2,12-dienes.
Endo-Selective Insertion by Norcaranylidene Carbenoid into the α-C-H Bond of Alkoxides: Evidence of a Hydride Abstraction-Recombination Mechanism
Oku, Akira,Yamaura, Yasunari,Harada, Toshiro
, p. 3730 - 3732 (2007/10/02)
A hydride abstraction-recombination mechanism in the insertion of the α-C-H bond of alkoxides by norcaranylidene carbenoid is proposed on the basis of the preferential endo stereoselectivity at the carbenic carbon of the insertion products
