96227-94-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound has a cyclic structure consisting of an ether linkage (oxygen atom) and a dioxepin ring (six-membered ring with two oxygen atoms). A cyclohexyl group (six-membered carbon ring) is also attached to the structure.
Explanation
Synonyms are alternative names for the same chemical compound, which can be used interchangeably.
Explanation
The compound is used as a starting material or intermediate in the synthesis of various drugs and medications due to its unique structural properties.
Explanation
The compound is also utilized in organic synthesis and serves as a reagent in chemical reactions, taking advantage of its specific structural features.
Explanation
Due to its chemical properties, the compound may pose risks to health or the environment if not handled and stored properly.
Explanation
To minimize the risks associated with the compound's hazardous nature, it is essential to follow appropriate safety protocols, including proper handling, storage, and disposal methods.
Chemical structure
Cyclic ether with a dioxepin ring and a cyclohexyl group
Synonyms
4-Cyclohexyl-4,7-dihydro-2,2-dimethyl-1,3-dioxepin
Application
Pharmaceutical industry as a building block for drug synthesis
Application
Organic synthesis and as a reagent in chemical reactions
Hazardous nature
Potentially hazardous
Safety precautions
Proper handling and storage procedures required
Check Digit Verification of cas no
The CAS Registry Mumber 96227-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,2 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96227-94:
(7*9)+(6*6)+(5*2)+(4*2)+(3*7)+(2*9)+(1*4)=160
160 % 10 = 0
So 96227-94-0 is a valid CAS Registry Number.
96227-94-0Relevant academic research and scientific papers
Stereoselective Syntheses of Alkenyl-Substituted 1,3-Dioxolanes or 4,7-Dihydro-1,3-dioxepins or an (E)-α,β-Unsaturated Aldehyde from (Z)-2-Butane-1,4-diols
Zweifel, George,Leung, Teresa,Najafi, M. Ramin,Najdi, Samir
, p. 2004 - 2006 (2007/10/02)
Treatment of (Z)-2-butene-1,4-diols with boron trifluoride etherate in acetone solvent affords stereodefined alkenyl-substituted 1,3-dioxolanes or 4,7-dihydro-1,3-dioxepins or an (E)-α,β-unsaturated aldehyde, depending on the reaction temperature and time
