6277-26-5 Usage
Uses
Used in Metalworking Fluids Industry:
ACETONE-BENZOTHIAZOLYL-2-HYDRAZONE is used as a corrosion inhibitor to protect metal surfaces from degradation during the manufacturing process, thereby enhancing the longevity and performance of metal components.
Used in Pharmaceutical and Agrochemical Industries:
ACETONE-BENZOTHIAZOLYL-2-HYDRAZONE serves as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides with improved efficacy and safety profiles.
Used in Antimicrobial Applications:
Leveraging its antimicrobial properties, ACETONE-BENZOTHIAZOLYL-2-HYDRAZONE is used in the formulation of antimicrobial coatings and paints, providing protection against microbial growth on surfaces in various settings, such as healthcare facilities and food processing plants.
Used in Organic Synthesis and Material Science:
Due to its unique reactivity, ACETONE-BENZOTHIAZOLYL-2-HYDRAZONE is utilized in organic synthesis for the development of new chemical compounds with potential applications in various industries. It also plays a role in material science, where it can be incorporated into the design and synthesis of novel materials with specific properties.
Used in Biological Detection Systems:
ACETONE-BENZOTHIAZOLYL-2-HYDRAZONE is being studied for its potential use as a fluorescent probe for detecting metal ions in biological systems, which could have significant implications for environmental monitoring, medical diagnostics, and other applications requiring sensitive and selective detection methods.
Check Digit Verification of cas no
The CAS Registry Mumber 6277-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6277-26:
(6*6)+(5*2)+(4*7)+(3*7)+(2*2)+(1*6)=105
105 % 10 = 5
So 6277-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3S/c1-7(2)12-13-10-11-8-5-3-4-6-9(8)14-10/h3-6H,1-2H3,(H,11,13)
6277-26-5Relevant academic research and scientific papers
Pharmaceutical preparation
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, (2008/06/13)
Pharmaceutical preparations having an antiphlogistic action are described. The preparations contain, as active ingredient, a benzazole derivative corresponding to the general tautomeric formulae I STR1 wherein X represents a sulphur or oxygen atom and R1 represents a hydrogen atom and R2 a hydroxymethyl, formyl, lower carbalkoxy or lower acyl group or R1 and R2 together represent the group STR2 wherein R3 and R4 denote, independently of one another, a hydrogen atom or a C1 -C6 -alkyl group, or they contain a physiologically acceptable salt thereof. These pharmaceutical preparations are suitable in particular for the treatment of inflammatory conditions and for inhibiting the lipoxygenase and/or cyclooxygenase route of arachidonic acid metabolism.
ETUDE DE LA FRAGMENTATION PAR IMPACT ELECTRONIQUE DE DERIVES DU BENZOTHIAZOLE
Claude, Saturnin,Tabacchi, Raffaele,Duc, Laurent,Fuchs, Rudolf,Boosen, Karl-Josef
, p. 682 - 692 (2007/10/02)
The mass spectra of eighteen substituted benzothiazoles are reported and discussed.All these compounds are thermodynamically stable and give an intense molecular ion, which undergoes different types of fragmentation depending on the nature of the substituent which is rarely eliminated directly. β-Cleavage with respect to the heterocyclic double bond is often obseved.Specific 2H-, 13C-, 15N- and 34S-labelling have been used in order to confirm the fragmentation patterns.
