392-10-9 Usage
Description
(2E)-2-[1-(2-fluorophenyl)ethylidene]hydrazinecarboxamide is an organic compound characterized by its chemical formula C9H10FN3O. It is a yellow solid with a molecular weight of 181.19 g/mol. (2E)-2-[1-(2-fluorophenyl)ethylidene]hydrazinecarboxamide is a hydrazinecarboxamide derivative, featuring a distinctive (2E)-2-[1-(2-fluorophenyl)ethylidene] group. It is frequently utilized in the realms of organic synthesis and medicinal chemistry research, and it holds promise for the development of pharmaceutical drugs aimed at treating a variety of diseases and medical conditions. Further research is essential to fully explore its properties and potential applications.
Uses
Used in Organic Synthesis:
(2E)-2-[1-(2-fluorophenyl)ethylidene]hydrazinecarboxamide is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for versatile reactions and the formation of a wide range of compounds.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (2E)-2-[1-(2-fluorophenyl)ethylidene]hydrazinecarboxamide is employed as a research compound to explore its potential in the development of new pharmaceutical drugs. Its specific structural features may contribute to the discovery of novel therapeutic agents.
Used in Pharmaceutical Drug Development:
(2E)-2-[1-(2-fluorophenyl)ethylidene]hydrazinecarboxamide is used as a precursor in the synthesis of pharmaceutical drugs, particularly for the treatment of various diseases and medical conditions. Its potential applications in drug development are currently under investigation, with the aim of identifying its therapeutic properties and efficacy.
Note: Since the provided materials do not specify particular applications or industries for (2E)-2-[1-(2-fluorophenyl)ethylidene]hydrazinecarboxamide, the uses listed are general and based on the compound's characteristics and common applications in related fields. Further research would be necessary to identify specific uses in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 392-10-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 392-10:
(5*3)+(4*9)+(3*2)+(2*1)+(1*0)=59
59 % 10 = 9
So 392-10-9 is a valid CAS Registry Number.
392-10-9Relevant articles and documents
Structure-activity relationship study of a novel necroptosis inhibitor, necrostatin-7
Zheng, Weihong,Degterev, Alexei,Hsu, Emily,Yuan, Junying,Yuan, Chengye
scheme or table, p. 4932 - 4935 (2009/05/26)
Necroptosis is a regulated caspase-independent cell death mechanism characterized by morphological features resembling non-regulated necrosis. Necrotatin-7 (Nec-7), a novel potent small-molecule inhibitor of necroptosis, is structurally distinct from previously described necrostatins (Nec-1, Nec-3, Nec-4 and Nec-5). Here, we describe a series of structural modifications and the structure-activity relationship (SAR) of the Nec-7 series for inhibiting necroptosis.
DIORGANOSILICON(IV) COMPLEXES OF FLUORO-IMINES: SYNTHETIC, SPECTROSCOPIC AND BIOLOGICAL ASPECTS
Saxena, Chitra,Singh, R. V.
, p. 17 - 26 (2007/10/02)
The synthetic, spectroscopic and biological studies of some diorganosilicon(IV) complexes derived from fluoroimines having NS and NO donor systems have been undertaken. The fluoroimines were prepared by the condensation of 2-Fluorobenzaldehyde and 1-(2-Fl
