Cas 1351465-53-6,N-(3-chloro-4-fluorophenyl)-N'-(pyridin-4-ylcarbonyl)hydrazonoformamide

1351465-53-6

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Basic information

Product Name: N-(3-chloro-4-fluorophenyl)-N'-(pyridin-4-ylcarbonyl)hydrazonoformamide
Synonyms: N-(3-chloro-4-fluorophenyl)-N'-(pyridin-4-ylcarbonyl)hydrazonoformamide
CAS NO:1351465-53-6
Molecular Formula:
Molecular Weight: 292.7
EINECS: N/A
Product Categories: N/A
Mol File: 1351465-53-6.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: N-(3-chloro-4-fluorophenyl)-N'-(pyridin-4-ylcarbonyl)hydrazonoformamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(3-chloro-4-fluorophenyl)-N'-(pyridin-4-ylcarbonyl)hydrazonoformamide(1351465-53-6)
EPA Substance Registry System: N-(3-chloro-4-fluorophenyl)-N'-(pyridin-4-ylcarbonyl)hydrazonoformamide(1351465-53-6)

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: 1351465-53-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1351465-53-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,1,4,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1351465-53:
(9*1)+(8*3)+(7*5)+(6*1)+(5*4)+(4*6)+(3*5)+(2*5)+(1*3)=146
146 % 10 = 6
So 1351465-53-6 is a valid CAS Registry Number.

1351465-53-6Upstream product

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1351465-53-6Relevant articles and documents

New series of isoniazid hydrazones linked with electron-withdrawing substituents

Vavrikova, Eva,Polanc, Slovenko,Kocevar, Marijan,Kosmrlj, Janez,Horvati, Kata,Bsze, Szilvia,Stolarikova, Jirina,Imramovsky, Ales,Vinsova, Jarmila

, p. 5902 - 5909 (2012/01/03)

A series of new isoniazid hydrazones was synthesized by two procedures. In the first isoniazid was activated with diethoxymethyl acetate and condensed with the appropriate anilines. Alternatively, substituted anilines were activated by diethoxymethyl acet

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