136440-59-0 Usage
Uses
Used in Pharmaceutical Research:
(Z)-2-amino-5-chlorobenzophenonamidinohydrazone acetate is used as a research compound for its potential anti-cancer properties, as it has been shown to inhibit the growth of cancer cells in various studies.
Used in Inflammatory Condition Treatment:
(Z)-2-amino-5-chlorobenzophenonamidinohydrazone acetate is used as a research compound for its potential anti-inflammatory properties, as it has demonstrated the ability to reduce inflammation in animal models.
Used in Enzyme Inhibition Studies:
(Z)-2-amino-5-chlorobenzophenonamidinohydrazone acetate is used as a research compound for studying its enzyme-inhibiting activity, which may contribute to its therapeutic potential in the treatment of various diseases.
Used in Drug Development:
(Z)-2-amino-5-chlorobenzophenonamidinohydrazone acetate is used as a starting point for the development of new medications aimed at treating cancer and inflammatory conditions, due to its demonstrated biological activities and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 136440-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,4 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136440-59:
(8*1)+(7*3)+(6*6)+(5*4)+(4*4)+(3*0)+(2*5)+(1*9)=120
120 % 10 = 0
So 136440-59-0 is a valid CAS Registry Number.
136440-59-0Relevant academic research and scientific papers
Antiarrhythmic active amidinohydrazones of substituted benzophenones. Part 5: Investigations on the stability of (Z)-2-amino-5-chlorobenzophenonamidinohydrazone acetate in solution
Schleuder,Richter,Keckeis,Jira
, p. 33 - 37 (2007/10/02)
The aqueous solution of the title compound can be used for injection for one year if it is stored at room temperature and under light protection. Under these conditions 8% of the E-isomer are produced. The reaction is reversible at day light. Red coloured products of decomposition are formed by long lasting influence of light. At higher temperatures or at sterilisation several products of decomposition are formed which structure is elucidated. For these decomposition a scheme is proposed.
Antiarrhythmic active amidinohydrazones of substituted benzophenones. Part 4: Investigations on photoisomerization of (Z)- and (E)-2-amino-5-chlorobenzophenonamidinohydrazone and the corresponding (E)-N-phenylamidinohydrazone
Richter,Schleuder,Geissler,Tomaschewski,Kasbohm
, p. 916 - 918 (2007/10/02)
The title compounds undergo a photoisomerization by irradiation. If the E-isomers are irradiated by light of a wavelength of an absorption maximum typical for them, they can be converted quantitatively to the corresponding Z-isomers. In case that the synt
