42067-67-4 Usage
Uses
Used in Pharmaceutical Research:
AKOS BC-0207 is used as a research compound for its potential applications in the development of pharmaceuticals. Its ability to inhibit certain enzymes makes it a candidate for further exploration in drug discovery processes.
Used in Organic Synthesis:
In the field of organic synthesis, AKOS BC-0207 is utilized as a reagent or intermediate. This role is crucial for the synthesis of more complex organic compounds, contributing to the advancement of chemical research and the creation of new materials.
Used in Cancer Research:
AKOS BC-0207 is studied for its potential as a treatment for cancer. Its inhibitory effects on enzymes suggest that it may have therapeutic benefits in managing or treating various types of cancer, warranting further investigation in medical research.
Used in Laboratory Settings:
AKOS BC-0207 is handled with caution in laboratory settings due to its chemical properties. It is essential to follow appropriate safety protocols when working with AKOS BC-0207 to ensure the safety of researchers and the integrity of experiments.
Check Digit Verification of cas no
The CAS Registry Mumber 42067-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42067-67:
(7*4)+(6*2)+(5*0)+(4*6)+(3*7)+(2*6)+(1*7)=104
104 % 10 = 4
So 42067-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H19N/c12-6-11-9-2-7-1-8(4-9)5-10(11)3-7/h7-11H,1-6,12H2
42067-67-4Relevant academic research and scientific papers
Synthesis and Reactions of 2-Adamantylidenenitromethane
Klimochkin,Leonova,Moiseev
, p. 494 - 498 (2007/10/03)
Synthesis of 2-adamantylidenenitromethane by nitration of 2-methyl-2-adamantanol was developed. Reaction of the 2-adamantylidenenitromethane with acids HX (X = ONO2, Cl, Br) yields the corresponding 2-X-adamantane-2-carboxylic acids, and under conditions of Ritter's reaction affords 2-acetylaminoadamantane-2-carboxylic acid. Reaction of the 2-adamantylidenenitromethane with nitric acid in a mixture with acetic anhydride occurs with carcass rearrangement and results in 4-exo-nitroxy-3-protoadamantanecarboxylic acid. The reduction of the nitroolefin with lithium aluminum hydride furnishes 2-aminomethyladamantane, and reaction with excess methylmagnesium iodide gives N-(2-methyl-2-adamantyl)methyl-N-hydroxylamine.
