144608-90-2 Usage
Derivative of cyclohexenamine
It is a modified version of the parent compound cyclohexenamine, with additional groups attached to it.
Heptenyl and methylpropyl groups attached
The compound has a heptenyl group (seven-carbon alkenyl group) and a 2-methylpropyl group (a branched three-carbon alkyl group) attached to the amine functional group.
(E)configuration
The compound has a trans (E) configuration at the double bond between the cyclohexenyl and heptenyl groups, indicating the arrangement of the substituents around the double bond.
Potential applications in organic synthesis
The compound may be useful as an intermediate or building block in organic synthesis, allowing for the creation of more complex molecules.
Potential applications in pharmaceutical research
The compound could have potential as a drug candidate or as a precursor to other bioactive molecules, but further studies are needed to determine its specific properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 144608-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,0 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144608-90:
(8*1)+(7*4)+(6*4)+(5*6)+(4*0)+(3*8)+(2*9)+(1*0)=132
132 % 10 = 2
So 144608-90-2 is a valid CAS Registry Number.
144608-90-2Relevant academic research and scientific papers
Stereochemical consequences of the Lewis acid-promoted 3-aza-cope rearrangement of N-alkyl-N-allyl enamines
Cook, Ggregory R.,Stille, John R.
, p. 4105 - 4124 (2007/10/02)
Internal and relative asymmetric induction were examined for the electrophile promoted 3-aza-Cope rearrangement of substituted N-alkyl-N-allyl enamines. In general, internal asymmetric induction was highly variable, and was dependent both upon the nature
Studies of Regiospecific 3-Aza-Cope Rearrangement Promoted by Electrophilic Reagents
Barta, Nancy S.,Cook, Gregory R.,Landis, Margaret S.,Stille, John R.
, p. 7188 - 7194 (2007/10/02)
The 3-aza-Cope rearrangement of N-alkyl-N-allyl enamine substrates, which required temperatures of 250 deg C to proceed thermally, was promoted at 111 deg C in the presence of electrophilic reagents such as HCl (0.5 equiv), TiCl4 (0.2 equiv), AlMe3 (1.2 e
