Cas 1417543-83-9,4-[(2-fluorophenyl)methyl]-5-oxo-2,5-dihydro-1H-pyrazole-1-carboximidamide

1417543-83-9

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Basic information

Product Name: 4-[(2-fluorophenyl)methyl]-5-oxo-2,5-dihydro-1H-pyrazole-1-carboximidamide
Synonyms: 4-[(2-fluorophenyl)methyl]-5-oxo-2,5-dihydro-1H-pyrazole-1-carboximidamide
CAS NO:1417543-83-9
Molecular Formula:
Molecular Weight: 234.233
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: 4-[(2-fluorophenyl)methyl]-5-oxo-2,5-dihydro-1H-pyrazole-1-carboximidamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(2-fluorophenyl)methyl]-5-oxo-2,5-dihydro-1H-pyrazole-1-carboximidamide(1417543-83-9)
EPA Substance Registry System: 4-[(2-fluorophenyl)methyl]-5-oxo-2,5-dihydro-1H-pyrazole-1-carboximidamide(1417543-83-9)

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: 1417543-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1417543-83-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,5,4 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1417543-83:
(9*1)+(8*4)+(7*1)+(6*7)+(5*5)+(4*4)+(3*3)+(2*8)+(1*3)=159
159 % 10 = 9
So 1417543-83-9 is a valid CAS Registry Number.

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1417543-83-9Relevant academic research and scientific papers

Heterocycles from Morita-Baylis-Hillman adducts: Synthesis of 5-oxopyrazolidines, arylidene-5-oxopyrazolidines, and oxo-2,5-dihydro-pyrazols

Correia, José Tiago M.,Rodrigues Jr., Manoel T.,Santos, Hugo,Tormena, Cláudio F.,Coelho, Fernando

, p. 826 - 832 (2013)

Starting from Morita-Baylis-Hillman (MBH) adducts, an approach for the synthesis of oxopyrazolidines, arylidene-oxopyrazolidines, and oxo-2,5-dihydropyrazoles is described. The method is based on a tandem process involving a Michael addition of amino-guan

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