Cas 1147846-97-6,ethyl 4-(4-(2-fluoro-4-nitrophenyl)piperazin-1-yl)-6-methyl-2-oxocyclohex-3-ene-1-carboxylate

1147846-97-6

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Basic information

Product Name: ethyl 4-(4-(2-fluoro-4-nitrophenyl)piperazin-1-yl)-6-methyl-2-oxocyclohex-3-ene-1-carboxylate
Synonyms:
CAS NO:1147846-97-6
Molecular Formula:
Molecular Weight: 405.426
EINECS: N/A
Product Categories: N/A
Mol File: 1147846-97-6.mol
Article Data: 1

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: ethyl 4-(4-(2-fluoro-4-nitrophenyl)piperazin-1-yl)-6-methyl-2-oxocyclohex-3-ene-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-(4-(2-fluoro-4-nitrophenyl)piperazin-1-yl)-6-methyl-2-oxocyclohex-3-ene-1-carboxylate(1147846-97-6)
EPA Substance Registry System: ethyl 4-(4-(2-fluoro-4-nitrophenyl)piperazin-1-yl)-6-methyl-2-oxocyclohex-3-ene-1-carboxylate(1147846-97-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1147846-97-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1147846-97-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,8,4 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1147846-97:
(9*1)+(8*1)+(7*4)+(6*7)+(5*8)+(4*4)+(3*6)+(2*9)+(1*7)=186
186 % 10 = 6
So 1147846-97-6 is a valid CAS Registry Number.

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1147846-97-6Relevant articles and documents

Synthesis, antibacterial and anticonvulsant evaluations of some cyclic enaminones

Edafiogho, Ivan O.,Phillips, Oludotun A.,Udo, Edet E.,Samuel, Santosh,Rethish, Beigy

, p. 967 - 975 (2009)

Several cyclic enaminone esters were synthesized, characterized, and evaluated for anticonvulsant and antibacterial activities using standardized tests. A series of enaminones were mainly phenyl analogs of anticonvulsant enaminones, while a second series

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