Cas 1394897-97-2,3-acetyl-5-(p-tolyl)-1-[(5-amino-4-cyano-1-phenylpyrazol-3-yl)ethylidene]-1,2-dihydroformazan

1394897-97-2

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Basic information

Product Name: 3-acetyl-5-(p-tolyl)-1-[(5-amino-4-cyano-1-phenylpyrazol-3-yl)ethylidene]-1,2-dihydroformazan
Synonyms:
CAS NO:1394897-97-2
Molecular Formula:
Molecular Weight: 414.47
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: 3-acetyl-5-(p-tolyl)-1-[(5-amino-4-cyano-1-phenylpyrazol-3-yl)ethylidene]-1,2-dihydroformazan(CAS DataBase Reference)
NIST Chemistry Reference: 3-acetyl-5-(p-tolyl)-1-[(5-amino-4-cyano-1-phenylpyrazol-3-yl)ethylidene]-1,2-dihydroformazan(1394897-97-2)
EPA Substance Registry System: 3-acetyl-5-(p-tolyl)-1-[(5-amino-4-cyano-1-phenylpyrazol-3-yl)ethylidene]-1,2-dihydroformazan(1394897-97-2)

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: 1394897-97-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394897-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,8,9 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1394897-97:
(9*1)+(8*3)+(7*9)+(6*4)+(5*8)+(4*9)+(3*7)+(2*9)+(1*7)=242
242 % 10 = 2
So 1394897-97-2 is a valid CAS Registry Number.

1394897-97-2Upstream product

1394897-97-2Downstream Products

1394898-04-4 2,6-dimethyl-3-[p-tolylazo]-8-phenyl-9-amino-imidazo[1,2-b]pyrazolo[4,3-d]pyridazine

1394897-97-2Relevant academic research and scientific papers

Synthesis and tautomeric structure of novel 3-arylazoimidazo[1,2-b] pyrazolo[4,3-d]pyridazines

Farghaly, Thoraya A.,Shawali, Ahmad Sami

, p. 296 - 299 (2012/10/08)

Treatment of 3-acetyl-5-amino-4-cyano-1-phenylpyrazole with hydrazine hydrate afforded the hydrazone derivative. Reaction of the latter hydrazone with hydrazonoyl chlorides was found to be site selective as it afforded the corresponding formazan and not t

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