Cas 395104-76-4,Benzamide, N-[(4-fluorophenyl)methyl]-3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenyl methyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]-

395104-76-4

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Basic information

Product Name: Benzamide, N-[(4-fluorophenyl)methyl]-3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenyl methyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]-
Synonyms:
CAS NO:395104-76-4
Molecular Formula: C47H39FN6O2
Molecular Weight: 738.864
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: Benzamide, N-[(4-fluorophenyl)methyl]-3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenyl methyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzamide, N-[(4-fluorophenyl)methyl]-3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenyl methyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]-(395104-76-4)
EPA Substance Registry System: Benzamide, N-[(4-fluorophenyl)methyl]-3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenyl methyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]-(395104-76-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 395104-76-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 395104-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,5,1,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 395104-76:
(8*3)+(7*9)+(6*5)+(5*1)+(4*0)+(3*4)+(2*7)+(1*6)=154
154 % 10 = 4
So 395104-76-4 is a valid CAS Registry Number.

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395104-76-4Relevant academic research and scientific papers

Indazole derivatives as JNK inhibitors and compositions and methods related thereto

-

, (2008/06/13)

Compounds having activity as selective inhibitors of JNK are disclosed. The compounds of this invention are indazole derivatives having the following structure: wherein R1, R2 and A are as defined herein. Such compounds have utility in the treatment of a wide range of conditions that are responsive to JNK inhibition. Thus, methods of treating such conditions are also disclosed, as are pharmaceutical compositions containing one or more compounds of the above compounds.

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