Cas 873958-18-0,(E)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-(furan-2-ylmethyleneamino)-1H-pyrazole-3-carbonitrile

873958-18-0

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Basic information

Product Name: (E)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-(furan-2-ylmethyleneamino)-1H-pyrazole-3-carbonitrile
Synonyms: (E)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-(furan-2-ylmethyleneamino)-1H-pyrazole-3-carbonitrile
CAS NO:873958-18-0
Molecular Formula:
Molecular Weight: 399.159
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: (E)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-(furan-2-ylmethyleneamino)-1H-pyrazole-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-(furan-2-ylmethyleneamino)-1H-pyrazole-3-carbonitrile(873958-18-0)
EPA Substance Registry System: (E)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-(furan-2-ylmethyleneamino)-1H-pyrazole-3-carbonitrile(873958-18-0)

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: 873958-18-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 873958-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,9,5 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 873958-18:
(8*8)+(7*7)+(6*3)+(5*9)+(4*5)+(3*8)+(2*1)+(1*8)=230
230 % 10 = 0
So 873958-18-0 is a valid CAS Registry Number.

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873958-18-0Relevant academic research and scientific papers

Design and synthesis of heterocyclic enamine derivatives based on skeleton of neonicotinoids

Liu, Chuanxiang,Yi, Fengping,Zou, Jianzhong

, p. 113 - 116 (2012)

Novel heterocyclic enamine derivatives based on skeleton of neonicotinoids were designed and prepar ed by the substitution reaction between heterocyclic enamines with intermediates of neonicotinoids, which provides readily accessible neonicotinoid analogs

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