Cas 95702-51-5,1-(4-dimethylamino-benzylidene)-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1<i>H</i>-pyrazol-4-yl)-thiosemicarbazide

95702-51-5

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Basic information

Product Name: 1-(4-dimethylamino-benzylidene)-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-thiosemicarbazide
Synonyms: 1-(4-dimethylamino-benzylidene)-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-thiosemicarbazide
CAS NO:95702-51-5
Molecular Formula:
Molecular Weight: 408.527
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(4-dimethylamino-benzylidene)-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-thiosemicarbazide(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-dimethylamino-benzylidene)-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-thiosemicarbazide(95702-51-5)
EPA Substance Registry System: 1-(4-dimethylamino-benzylidene)-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-thiosemicarbazide(95702-51-5)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 95702-51-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95702-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,0 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95702-51:
(7*9)+(6*5)+(5*7)+(4*0)+(3*2)+(2*5)+(1*1)=145
145 % 10 = 5
So 95702-51-5 is a valid CAS Registry Number.

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95702-51-5Relevant academic research and scientific papers

New thiazolidones-4 with pyrazolone-5 substituent as the potential NSAIDs

Lesyk,Vladzimirska,Zimenkovsky,Horishny,Nektegayev,Solyanyk,Vovk

, p. 210 - 217 (2007/10/03)

The synthesis of a group of thiazolidine derivatives with pyrazolone-5 substituent is described. The structure of the new compounds is supported by 1H- and 13C-NMR spectra. Group of compounds was tested in vivo for their antiinflammatory activity. The obtained results gave the opportunity to separate the perspective groups of potential NSAIDs, which have got greater antiinflammatory activity than the best standard drugs.

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