96554-86-8 Usage
Chemical structure
A complex and specific structure with a 15-methyl group, an 8-aza ring, and a 16-oxagona-1,3,5(10),13-tetraen-17-one backbone.
Functional groups
Contains aza and oxagona functional groups, which may contribute to potential pharmaceutical or biological activity.
Potential applications
Due to the presence of aza and oxagona functional groups, this compound may have potential pharmaceutical or biological activity, although further research is needed to determine its exact properties and potential uses.
Uniqueness
The compound's unique structure makes it an interesting subject for further study and analysis.
Need for further information
Without additional information, it is difficult to determine the exact properties and potential uses of this compound.
Please note that this list is based on the limited information provided in the material. A more comprehensive understanding of the compound's properties and potential applications would require further research and analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 96554-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,5 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96554-86:
(7*9)+(6*6)+(5*5)+(4*5)+(3*4)+(2*8)+(1*6)=178
178 % 10 = 8
So 96554-86-8 is a valid CAS Registry Number.
96554-86-8Relevant articles and documents
HETEROCYCLIC ANALOGS OF STEROIDS. XIV. SYNTHESIS OF CONJUGATED ENAMINO LACTONES OF THE 8-AZA-16-OXASTEROID SERIES AND SOME OF THEIR CHARACTERISTICS
Akhrem, A.A.,Lakhvich, F.A.,Lis, L.G.,Kuz'mitskii, B.B.,Mizulo, N.A.,Gorbacheva, I.A.
, p. 1227 - 1232 (2007/10/02)
Methods are proposed for the synthesis of enamino lactones of the 8-aza-16-oxasteroid series from the corresponding enamino ketolactones, involving either the intermediate production of the thioketals with subsequent sulfurization or direct regiospecific reduction under the conditions of ionic hydrogenation.The stereochemistry of the products is examined, and data on their biological activity is given.
