5449-28-5 Usage
Uses
Used in Pharmaceutical Applications:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide is used as a pharmaceutical candidate for its potential applications in medicinal chemistry. Its hydrazine and amide functional groups make it a promising compound for targeting various biological activities.
Used in Medicinal Chemistry Research:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide is used as a subject of ongoing research for its potential applications in medicinal chemistry. Its unique structure and functional groups allow for exploration of its interactions with biological systems and potential therapeutic uses.
Used in Synthetic Chemistry:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide is used as an important chemical in synthetic chemistry. Its hydrazine and amide functional groups can be utilized in the synthesis of various compounds with potential applications in different fields.
Used in Drug Development:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide is used as a potential lead compound in drug development. Its unique structure and functional groups can be optimized and modified to develop new drugs with improved efficacy and safety profiles.
Used in Chemical Synthesis:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide is used as a starting material or intermediate in the synthesis of various organic compounds. Its hydrazine and amide functional groups can be further modified or reacted with other reagents to produce a wide range of chemical products.
Used in Chemical Analysis:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide can be used as a reference compound or standard in chemical analysis and testing. Its unique structure and properties can be utilized for the development of analytical methods and techniques.
Used in Material Science:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide may have potential applications in material science, such as in the development of new materials with specific properties or functions. Its hydrazine and amide functional groups can be incorporated into polymers, coatings, or other materials to enhance their performance.
Used in Environmental Applications:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide may have potential applications in environmental science, such as in the development of new methods for pollution control or remediation. Its unique structure and functional groups can be utilized to target specific contaminants or pollutants.
Used in Analytical Chemistry:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide can be used as a reagent or catalyst in various analytical chemistry processes. Its hydrazine and amide functional groups can facilitate specific chemical reactions or improve the efficiency of analytical techniques.
Used in Chemical Education:
(2E)-2-(2,2-diphenylethylidene)hydrazinecarboxamide can be used as a teaching aid in chemical education to illustrate the principles of organic chemistry, functional groups, and chemical reactions. Its unique structure and properties can help students understand the concepts and applications of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 5449-28-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5449-28:
(6*5)+(5*4)+(4*4)+(3*9)+(2*2)+(1*8)=105
105 % 10 = 5
So 5449-28-5 is a valid CAS Registry Number.
5449-28-5Relevant academic research and scientific papers
Synthesis of novel indole hydrazone derivatives and evaluation of their antiplatelet aggregation activity
Mashayekhi, Vida,Tehrani, Kamaleddin Haj Mohammad Ebrahim,Amidi, Salimeh,Kobarfard, Farzad
, p. 144 - 150 (2013/03/28)
Based on the existing reports regarding the antiplatelet aggregation activity of hydrazone derivatives, a series of indole hydrazone derivatives were considered as potential antiplatelet agents and synthesized. The structures of the synthesized compounds
Carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones and the use thereof
-
, (2008/06/13)
This invention is related to carbocyclic and heterocyclic substituted semicarbazones and thiosemicarbazones represented by Formula I: or a pharmaceutically acceptable salt or prodrug thereof, wherein: Y is oxygen or sulfur; R1, R21, R22 and R23 are independently hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, haloalkyl, aryl, aminoalkyl, hydroxyalkyl, alkoxyalkyl or carboxyalkyl; or R22 and R23, together with the N, form a heterocycle; A1 and A2 are independently aryl, heteroaryl, saturated or partially unsaturated carbocycle or saturated or partially unsaturated heterocycle, any of which is optionally substituted; X is one or O, S, NR24, CR25R26, C(O), NR24C(O), C(O)NR24, SO, SO2 or a covalent bond; where R24, R25 and R26 are independently hydrogen, alkyl, cycloalkyl, alkenyl, alkynyl, haloalkyl, aryl, aminoalkyl, hydroxyalkyl, alkoxyalkyl or carboxyalkyl. The invention also is directed to the use of carbocycle and heterocycle substituted semicarbazones and thiosemicarbazones for the treatment of neuronal damage following global and focal ischemia, for the treatment or prevention of neurodegenerative conditions such as amyotrophic lateral sclerosis (ALS), for the treatment and prevention of otoneurotoxicity and eye diseases involving glutamate toxicity and for the treatment, prevention or amelioration of pain, as anticonvulsants, and as antimanic depressants, as local anesthetics, as antiarrhythmics and for the treatment or prevention of diabetic neuropathy and urinary incontinence.
