77173-67-2 Usage
Uses
ETHYL 4-CHLORO-8-CYANOQUINOXALINE-3-CARBOXYLATE is used as a chemical intermediate in various chemical synthesis processes due to its unique structural features and functional groups.
Used in Pharmaceutical Industry:
ETHYL 4-CHLORO-8-CYANOQUINOXALINE-3-CARBOXYLATE is used as a building block for the synthesis of pharmaceutical compounds, potentially contributing to the development of new drugs with specific therapeutic properties.
Used in Chemical Research:
In the field of chemical research, ETHYL 4-CHLORO-8-CYANOQUINOXALINE-3-CARBOXYLATE serves as a subject for studying the properties and reactions of chloroquinoxaline-based compounds, which may lead to the discovery of novel applications and insights into related chemical structures.
Used in Material Science:
ETHYL 4-CHLORO-8-CYANOQUINOXALINE-3-CARBOXYLATE may be utilized in the development of new materials with specific properties, such as conductivity, stability, or reactivity, depending on its interaction with other compounds and its structural characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 77173-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,7 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77173-67:
(7*7)+(6*7)+(5*1)+(4*7)+(3*3)+(2*6)+(1*7)=152
152 % 10 = 2
So 77173-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H9ClN2O2/c1-2-18-13(17)10-7-16-12-8(6-15)4-3-5-9(12)11(10)14/h3-5,7H,2H2,1H3
77173-67-2Relevant academic research and scientific papers
Design and synthesis of substituted quinolines as novel and selective melanin concentrating hormone antagonists as anti-obesity agents
Warshakoon, Namal C.,Sheville, Justin,Bhatt, Ritu Tiku,Ji, Wei,Mendez-Andino, Jose L.,Meyers, Kenneth M.,Kim, Nick,Wos, John A.,Mitchell, Chrissy,Paris, Jennifer L.,Pinney, Beth B.,Reizes, Ofer,Hu, X. Eric
, p. 5207 - 5211 (2007/10/03)
A novel series of substituted quinoline analogs were designed and synthesized as potent and selective melanin concentrating hormone (MCH) antagonists. These analogs show potent (nM) activity (12a-k) with a moderate selectivity. Conversely, the conformatio
