74803-32-0 Usage
Uses
Used in Pharmaceutical Industry:
8-Chloro-[1,2,4]triazolo[1,5-a]pyrazine is used as an active pharmaceutical ingredient for its potential anti-inflammatory and anti-cancer properties. It is being studied for its ability to modulate various biological pathways and processes that contribute to inflammation and cancer progression.
Used in Agricultural Industry:
In the agricultural sector, 8-CHLORO-[1,2,4]TRIAZOLO[1,5-A]PYRAZINE is utilized as a precursor in the synthesis of new pesticides and herbicides. Its bioactive nature makes it a valuable component in developing effective and targeted crop protection agents.
Used in Chemical Synthesis:
8-Chloro-[1,2,4]triazolo[1,5-a]pyrazine is also used as a chemical intermediate in the synthesis of novel pharmaceutical compounds. Its unique structure allows for the development of new molecules with potential therapeutic applications.
It is crucial to handle 8-CHLORO-[1,2,4]TRIAZOLO[1,5-A]PYRAZINE with care due to its potential hazards if not used properly, ensuring safety in both research and application settings.
Check Digit Verification of cas no
The CAS Registry Mumber 74803-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74803-32:
(7*7)+(6*4)+(5*8)+(4*0)+(3*3)+(2*3)+(1*2)=130
130 % 10 = 0
So 74803-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H3ClN4/c6-4-5-8-3-9-10(5)2-1-7-4/h1-3H
74803-32-0Relevant academic research and scientific papers
CXCR7 ANTAGONISTS
-
, (2014/06/23)
Compounds having formula I, or pharmaceutically acceptable salts, hydrates or N-oxides thereof are provided and are useful for binding to CXCR7, and treating diseases that are dependent, at least in part, on CXCR7 activity. Accordingly, the present invention provides in further aspects, compositions containing one or more of the above-noted compounds in admixture with a pharmaceutically acceptable excipient.
Ring Opening or Rearrangement versus N-Oxidation in the Action of Peracids upon Pyrrolopyridines, Pyrrolopyrazines, and Triazolo- and Triazolo-pyrazine. Some Chemical and Spectroscopic Properties of the Triazolopyrazines and Th
Hardy, Christopher R.,Parrick, John
, p. 506 - 511 (2007/10/02)
Peracid oxidation of the title heterocycles has shown a variety of reaction pathways. 1-Methyl-2,3-diphenyl-1H-pyrrolopyridine (8) gave a ring-opening product (13), while 3-methyl-2-phenyl-1H-pyrrolopyrazine gave N-benzoylurea.In contrast, t
