5382-85-4 Usage
Uses
Used in Organic Synthesis:
2-(cinnamylideneamino)guanidine is utilized as a reagent in chemical reactions, playing a crucial role in the synthesis of various organic compounds. Its unique structure allows for versatile reactions and the formation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-(cinnamylideneamino)guanidine is employed as a key component in the development of new drugs. Its antimicrobial and antifungal properties make it a promising candidate for the creation of novel treatments against infectious diseases.
Used in Antimicrobial Applications:
2-(cinnamylideneamino)guanidine is used as an antimicrobial agent, targeting a broad spectrum of microorganisms. Its ability to inhibit the growth of bacteria and fungi makes it a valuable asset in the fight against drug-resistant infections.
Used in Antifungal Applications:
Similarly, 2-(cinnamylideneamino)guanidine is used as an antifungal agent, effective against various fungal species. Its potential to combat fungal infections contributes to its significance in the pharmaceutical industry.
Used in Neurological Disorder Treatment:
2-(cinnamylideneamino)guanidine has been found to have potential in the treatment of certain neurological disorders. Its interaction with specific receptor sites in the brain suggests that it could be used as a therapeutic agent for conditions such as Alzheimer's disease, Parkinson's disease, or other neurodegenerative disorders.
Overall, 2-(cinnamylideneamino)guanidine is a versatile compound with a broad range of applications in the fields of chemistry and medicine, making it a valuable asset in research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 5382-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5382-85:
(6*5)+(5*3)+(4*8)+(3*2)+(2*8)+(1*5)=104
104 % 10 = 4
So 5382-85-4 is a valid CAS Registry Number.
5382-85-4Relevant academic research and scientific papers
Synthesis, Antileishmanial Activity and In Silico Studies of Aminoguanidine Hydrazones (AGH) and Thiosemicarbazones (TSC) Against Leishmania chagasi Amastigotes
Alexandre-Moreira, Magna S.,Aquino, Pedro G. V.,Bourguignon, Jean-Jacques,Bri-Card, Jacques,Freitas, Johnnatan D.,Meneghetti, Mario R.,Nascimento, Igor J. S.,Queiroz, Aline C.,Rodrigues, Klinger A. F.,Rodrigues, Raiza R. L.,Santos, Mariana S.,Schmitt, Martine,de Aquino, Thiago M.,Araújo, Morgana V.,Fran?a, Paulo H. B.,Rodrigues, érica E. E. S.,Santos-Júnior, Paulo F. S.,da Silva-Júnior, Edeildo F.,de Araújo-Júnior, Jo?o X.
, p. 151 - 169 (2022/02/05)
Background: Leishmaniasis is a worldwide health problem, highly endemic in developing countries. Among the four main clinical forms of the disease, visceral leishmaniasis is the most se-vere, fatal in 95% of cases. The undesired side-effects from first-li
ALKYLIDENE AMINOGUANIDINE AND SALT THEREOF, MODIFYING COMPOSITION, MODIFIED RUBBER FOR TIRE, RUBBER COMPOSITION FOR TIRE, AND TIRE
-
Paragraph 0116-0117, (2017/05/28)
Provided is a compound represented by formula (1): wherein X is an acid to form a salt with a guanidine site; and R1 and R2 are each independently any selected from the group consisting of a hydrogen atom, a C1-18 alkyl group, a cycloalkyl group, an aryl group, an alkylaryl group, and an alkenyl group, each of the groups optionally having one or more substituents each containing a sulfur atom, a nitrogen atom, or an oxygen atom.
Synthesis of aryl-hydrazones via ultrasound irradiation in aqueous medium
Leite, Ana Cristina Lima,Moreira, Diogo Rodrigo de M.,Coelho, Lucas Cunha Duarte,de Menezes, Frederico Duarte,Brondani, Dalci José
, p. 1538 - 1541 (2008/09/19)
The synthesis of aryl-hydrazones from aromatic aldehydes/ketones and hydrazides (semicarbazide, thiosemicarbazide and aminoguanidine) is described using aqueous medium (acid conditions) under ultrasound irradiation with short reaction times (20-30 min), t
