Cas 70014-67-4,7-acetyl-4b,6a-dichloro-5,5,6,6-tetrafluoro-2-phenyl-4a,4b,5,6,6a,7-hexahydro-cyclobuta[3,4]pyrazolo[1,5-<i>b</i>]pyridazine

70014-67-4

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Basic information

Product Name: 7-acetyl-4b,6a-dichloro-5,5,6,6-tetrafluoro-2-phenyl-4a,4b,5,6,6a,7-hexahydro-cyclobuta[3,4]pyrazolo[1,5-b]pyridazine
Synonyms: 7-acetyl-4b,6a-dichloro-5,5,6,6-tetrafluoro-2-phenyl-4a,4b,5,6,6a,7-hexahydro-cyclobuta[3,4]pyrazolo[1,5-b]pyridazine
CAS NO:70014-67-4
Molecular Formula:
Molecular Weight: 408.182
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: 7-acetyl-4b,6a-dichloro-5,5,6,6-tetrafluoro-2-phenyl-4a,4b,5,6,6a,7-hexahydro-cyclobuta[3,4]pyrazolo[1,5-b]pyridazine(CAS DataBase Reference)
NIST Chemistry Reference: 7-acetyl-4b,6a-dichloro-5,5,6,6-tetrafluoro-2-phenyl-4a,4b,5,6,6a,7-hexahydro-cyclobuta[3,4]pyrazolo[1,5-b]pyridazine(70014-67-4)
EPA Substance Registry System: 7-acetyl-4b,6a-dichloro-5,5,6,6-tetrafluoro-2-phenyl-4a,4b,5,6,6a,7-hexahydro-cyclobuta[3,4]pyrazolo[1,5-b]pyridazine(70014-67-4)

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: 70014-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 70014-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70014-67:
(7*7)+(6*0)+(5*0)+(4*1)+(3*4)+(2*6)+(1*7)=84
84 % 10 = 4
So 70014-67-4 is a valid CAS Registry Number.

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70014-67-4Relevant academic research and scientific papers

1,3-Dipolar Cycloaddition of Pyridazinium Ylides with Perhalocycloalkenes and Thermal Decomposition of the Adducts

Ohsawa, Akio,Wada, Ikuo,Igeta, Hiroshi

, p. 1023 - 1031 (2007/10/02)

Some pyridazinium N-ylides underwent 1,3-dipolar cycloaddition with perhalocyclopropenes and with a perhalocyclobutene.Thermal decomposition and chemical transformations of the pyrolyzed products afforded various hitherto unknown 2-chloropyrazolopyridazine derivatives.Keywords - pyridazinium N-ylide; pyridazine N-acylimine; N-acyliminopyridazine; 1,3-dipolar cycyloaddition; thermal ring-opening; diazaindolizine; pyrazolopyridazine; 2-chloropyrazolopyridazine.

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