92608-26-9 Usage
Chemical structure
A spiro compound with a diaza ring and a carbonyl group.
Molecular weight
168.24 g/mol
Diaza ring
A six-membered ring containing two nitrogen atoms.
Carbonyl group
A carbon-oxygen double bond (C=O) that is part of a larger molecule.
Pharmaceutical and drug synthesis
Due to its complex molecular structure and functional groups, it may have potential applications in the development of new drugs.
Organic synthesis
It can be used as a building block in the synthesis of more complex organic compounds.
Reactivity
The presence of the diaza ring and carbonyl group may make the compound reactive towards various reagents, which can be exploited in chemical reactions and drug synthesis.
Research interest
Researchers and chemists are interested in studying the structure, properties, and reactivity of this compound to explore its potential as a drug candidate or in organic synthesis.
Drug development
Understanding the properties and reactivity of this compound can aid in the development of new drugs with unique properties.
Physical state
Likely a solid at room temperature, given its molecular weight and structure.
Solubility
The compound's solubility in various solvents can be an important factor in its synthesis and application.
Safety and handling
As with any chemical compound, appropriate safety measures should be taken when handling and working with 1,7-Diazaspiro[4.5]decan-6-one,1-methyl-(9CI), including the use of personal protective equipment and proper disposal methods.
Check Digit Verification of cas no
The CAS Registry Mumber 92608-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,0 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92608-26:
(7*9)+(6*2)+(5*6)+(4*0)+(3*8)+(2*2)+(1*6)=139
139 % 10 = 9
So 92608-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H16N2O/c1-11-7-3-5-9(8(11)12)4-2-6-10-9/h10H,2-7H2,1H3
92608-26-9Relevant articles and documents
Spiro- and Bicyclic Azalactams by Hydrolysis of α-Chlorinated Bicyclic Amidines
Loefas, Stefan,Ahlberg, Per
, p. 583 - 586 (2007/10/02)
The synthetic potential of α-chlorinated bicyclic amidines to form spiro- and bicyclic azalactams on hydrolysis has been investigated.Thus, 2a,b, prepared by chlorination of 1a,b with carbon tetrachloride in DMF, were treated with water via hydrolysis of the amidine function and an intramolecular substitution, 2a, afforded the azaspirolactam 6a, and 2b gave the isomers 6b and 6c in the ratio 22:78, respectively.Similarly, α-chlorinated DBU 3b gave the bicyclic azalactam 10.A high-yield preparative method for obtaining the bicyclic amidine 1a was worked out on the basis of Reissert's method from 1893, starting from diethyl malonate and α-bromopropylphthalimide.
