5044-10-0 Usage
Quinazoline derivative
Contains a benzoquinazoline ring system.
Two dimethyl groups
These groups are attached to the 11a and 13a positions of the molecule.
Dione functional group
A carbonyl group (C=O) is present at the 2 and 8 positions of the molecule.
Multiple cyclohexane rings
The compound has several six-membered carbon rings in its structure.
Cyclic compound
The molecule forms a closed loop or ring.
Highly fused and complex structure
The compound has a complicated arrangement of its atoms and bonds.
Potential pharmaceutical or medicinal applications
Due to its unique structure and chemical properties, it may have uses in the development of drugs or medicines.
Further research and analysis needed
To determine the specific uses and effects of the compound, additional studies are required.
Check Digit Verification of cas no
The CAS Registry Mumber 5044-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,4 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5044-10:
(6*5)+(5*0)+(4*4)+(3*4)+(2*1)+(1*0)=60
60 % 10 = 0
So 5044-10-0 is a valid CAS Registry Number.
5044-10-0Relevant academic research and scientific papers
Beckmann rearrangement of 3-aza-A-homo-4α-androsten-4,17-dione oxime and 3-oxo-13α-amino-13,17-seco-4-androsten-17-oic 13,17-lactam oxime
Camoutsis,Catsoulacos
, p. 1093 - 1094 (2007/10/02)
Rearragements of 3-aza-A-homo-4α-androsten-4,17-dione oxime produced a mixture of the normal lactam product and the product of a 'second order' cleavage, an unsaturated nitrile. The lactam 3,17α-diaza-A,D-bishomoandrost-4α-ene-4,17-dione was also obtained from the rearrangement of the syn-3-oxo-13α-amino-13,17-seco-4-androsten-17-oic-13,17-lactam oxime. The resolution of syn- and anti-isomers of VIII was effected by column chromatography and their structure was determined by spectral data.
