16679-95-1 Usage
Uses
Used in Pharmaceutical Research:
Z-TYR-NHNH2 is utilized as a research compound for exploring its potential interactions with biological systems, given its combination of a biologically significant amino acid and a chemically reactive inorganic group. Its role in this context is to aid scientists in understanding how such a compound might influence neurotransmitter pathways or be developed into a therapeutic agent.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Z-TYR-NHNH2 serves as a starting point for the design and synthesis of new pharmaceuticals. Z-TYR-NHNH2's structure may offer insights into the development of drugs targeting specific receptors or enzymes, particularly those involved in the metabolism of neurotransmitters.
Used in Industrial Processes:
Although not explicitly stated in the provided materials, given that hydrazine is used in various industrial processes, Z-TYR-NHNH2 might also find applications in these areas. However, the specific industrial uses would require further investigation due to the compound's potential health and safety implications related to the hydrazine component.
Check Digit Verification of cas no
The CAS Registry Mumber 16679-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,7 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16679-95:
(7*1)+(6*6)+(5*6)+(4*7)+(3*9)+(2*9)+(1*5)=151
151 % 10 = 1
So 16679-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H19N3O4/c18-20-16(22)15(10-12-6-8-14(21)9-7-12)19-17(23)24-11-13-4-2-1-3-5-13/h1-9,15,21H,10-11,18H2,(H,19,23)(H,20,22)
16679-95-1Relevant academic research and scientific papers
An efficient, stereocontrolled and versatile synthetic route to bicyclic partially saturated privileged scaffolds
Bond, Andrew D.,Hanby, Abigail R.,King, Thomas A.,Moss, Thomas A.,Sore, Hannah F.,Spring, David R.,Stewart, Hannah L.
supporting information, p. 6818 - 6821 (2020/07/04)
Herein, we describe the development of a simple, high yielding and stereocontrolled strategy for the synthesis of a series of triazolopiperazines and other biologically relevant fused scaffolds from optically active amino acids. This route was applied to the synthesis of 22 scaffolds containing new, previously inaccessible vectors and used to access a novel analogue of ganaplacide.
