5757-96-0 Usage
Hydrazine derivative
It is a compound derived from hydrazine (N2H4) This indicates that the compound has a similar structure to hydrazine, with some modifications.
Mainly used in research and development
It is primarily utilized in scientific studies and the development of new compounds This highlights the compound's current stage of application, which is focused on further exploration and understanding.
Potential building block for the synthesis of new pharmaceuticals
It can be used as a starting material or intermediate in the creation of new drugs This suggests that the compound has the potential to be a valuable component in the development of future medications.
Applications in cancer treatment
It is being explored for its possible use in the development of cancer therapies This indicates that the compound may have potential benefits in the fight against cancer.
Further research needed
More studies are required to fully understand its properties and potential uses This emphasizes that the compound's potential is not yet fully realized and that continued research is necessary to unlock its full potential.
Check Digit Verification of cas no
The CAS Registry Mumber 5757-96-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5757-96:
(6*5)+(5*7)+(4*5)+(3*7)+(2*9)+(1*6)=130
130 % 10 = 0
So 5757-96-0 is a valid CAS Registry Number.
5757-96-0Relevant academic research and scientific papers
Synthesis of isoquinolines via Rh(III)-catalyzed C-H activation using hydrazone as a new oxidizing directing group
Chuang, Sheng-Chieh,Gandeepan, Parthasarathy,Cheng, Chien-Hong
supporting information, p. 5750 - 5753 (2013/12/04)
An efficient and mechanistically interesting method for the synthesis of highly substituted isoquinolines by a Rh(III)-catalyzed hydrazone directed ortho C-H bond activation and annulation without an external oxidant is described. This reaction is accomplished via a C-C and C-N bond formation along with N-N bond cleavage.
