419555-44-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the physical appearance of the compound, which is important for its identification and handling.
Explanation
This indicates the main area of application for the compound, which is in the development of new drugs and therapies.
Explanation
This suggests that the compound has not yet been proven to be effective in treating diseases, but it is being studied for this purpose.
Explanation
This means that the compound may help to reduce inflammation, which is a common symptom of many diseases.
Explanation
This means that the compound may help to protect cells from damage caused by free radicals, which can contribute to the development of various diseases.
Explanation
This indicates that more work is needed to determine the full range of potential uses and benefits of the compound, as well as any potential risks or side effects.
Appearance
White to off-white crystalline powder
Primary Use
Pharmaceutical research and development
Potential Medicinal Properties
Being investigated for its potential as a therapeutic agent in the treatment of various diseases
Anti-inflammatory Properties
Known to have some anti-inflammatory properties
Antioxidant Properties
Known to have some antioxidant properties
Further Research and Testing
Necessary to fully understand its potential applications and benefits
Check Digit Verification of cas no
The CAS Registry Mumber 419555-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,9,5,5 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 419555-44:
(8*4)+(7*1)+(6*9)+(5*5)+(4*5)+(3*5)+(2*4)+(1*4)=165
165 % 10 = 5
So 419555-44-5 is a valid CAS Registry Number.
419555-44-5Relevant academic research and scientific papers
Clark,Hodgson,Goldsmith,Blake,Cooke,Street
, p. 3325 - 3337 (2001)
Ammonium ylides produced by intramolecular reaction of copper carbenoids tethered to cyclic allylic amines undergo [2,3]-rearrangement to deliver bicyclic amines. The reaction can be performed using a cyclic N-allylamine in which the diazo group is tethered adjacent to nitrogen, or a vinyl-substituted cyclic amine in which the diazo group is N-tethered to the ring. In the former type of reaction, stereoselective ylide formation and rearrangement usually delivers high levels of diastereocontrol. In the latter case, efficient 'chirality transfer' can be accomplished when the reaction is performed using an enantiomerically pure substrate. The reactions have been used to construct pyrrolizidine, indolizidine and quinolizidine systems, and the CE sub-unit found in the manzamine and ircinal alkaloids.
