7496-99-3 Usage
General Description
2-methylazepane, also known as dimethylpiperidine, is a six-membered heterocyclic compound with a nitrogen atom. It is classified as an azepane and contains a methyl group at the 2-position of the ring. 2-methylazepane has potential applications in the field of organic synthesis and pharmaceuticals due to its unique structure and properties. It is used as a building block for the synthesis of various compounds and is also being investigated for its potential medicinal properties. 2-methylazepane has been studied for its potential as a central nervous system depressant and has also been explored for its potential use in the treatment of conditions such as epilepsy and Parkinson's disease. Overall, 2-methylazepane is a versatile compound with potential applications in both the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 7496-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7496-99:
(6*7)+(5*4)+(4*9)+(3*6)+(2*9)+(1*9)=143
143 % 10 = 3
So 7496-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N/c1-7-5-3-2-4-6-8-7/h7-8H,2-6H2,1H3
7496-99-3Relevant articles and documents
REDUCTION OF CONJUGATED CYCLOHEXENONE OXIMES WITH ALUMINIUM HYDRIDE
Zaidlewicz, Marek,Uzarewicz, Ireneusz G.
, p. 143 - 150 (2007/10/02)
The reduction of representative conjugated cyclohexenone oximes with aluminium hydride in tetrahydrofuran yields 2-cyclohexenylamines and saturated aziridines - 7-azabicycloheptane derivatives, as the main reaction products.Small quantities of cyclohexylamines and perhydroazepines are also formed.Regioselectivity of the reduction depends on oxime configuration.Higher yields of 2-cyclohexenylamines are obtained from E than Z isomers.The reaction mechanism is proposed.
