16041-56-8 Usage
Uses
Used in Organic Synthesis:
(2R,4AR,8AR)-2-METHYLOCTAHYDRO-4(1H)-QUINOLINONE is used as a building block in organic synthesis for the preparation of other complex molecules. Its unique structure allows for the creation of a wide range of compounds with diverse properties and applications.
Used in Medicinal Chemistry:
(2R,4AR,8AR)-2-METHYLOCTAHYDRO-4(1H)-QUINOLINONE is potentially useful in medicinal chemistry due to its structural features. Its quinolines framework may contribute to the development of new pharmaceuticals with various therapeutic effects.
Used in Pharmaceutical Research:
(2R,4AR,8AR)-2-METHYLOCTAHYDRO-4(1H)-QUINOLINONE may have biological activity that could be of interest for pharmaceutical research. Its potential applications in drug discovery and development make it a valuable candidate for further investigation.
Used in Industrial Applications:
(2R,4AR,8AR)-2-METHYLOCTAHYDRO-4(1H)-QUINOLINONE may have other industrial applications, such as in the production of fine chemicals or specialty materials. Its unique properties and versatility make it suitable for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 16041-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16041-56:
(7*1)+(6*6)+(5*0)+(4*4)+(3*1)+(2*5)+(1*6)=78
78 % 10 = 8
So 16041-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO/c1-7-6-10(12)8-4-2-3-5-9(8)11-7/h7-9,11H,2-6H2,1H3/t7-,8-,9-/m1/s1
16041-56-8Relevant academic research and scientific papers
STEREOCHEMISTRY OF NITROGEN HETEROCYCLES. 67. TRANSFORMATIONS OF STEREOISOMERIC 1-CHLORO-2-METHYL-4-KETO-trans-DECAHYDROQUINOLINES IN AN ACIDIC MEDIUM
Litvinenko, G. S.,Voronenko, L. A.,Isakova, L. A.
, p. 906 - 913 (2007/10/02)
It is shown that epimeric 1-chloro-2-methyl-4-keto-trans-decahydroquinolines in an acidic medium undergo intermolecular monochlorination in the α position relative to the carbonyl group with the formation of epimeric 3e-chloro- and 10a-chloro-2-methyl-4-keto-trans-decahydroquinolines and 2-methyl-4-keto-10-chloro-cis-decahydroquinolines.The mechanism of the transformations is examined, and an assumption regarding the possibility of cis-trans isomerization of the intermediately formed ?-chloronium complex is expressed.
