Cas 78026-30-9,3-Methyl-5-oxo-4-(phenyl-hydrazono)-4,5-dihydro-pyrazole-1-carbothioic acid phenylamide

78026-30-9

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Basic information

Product Name: 3-Methyl-5-oxo-4-(phenyl-hydrazono)-4,5-dihydro-pyrazole-1-carbothioic acid phenylamide
Synonyms: 3-Methyl-5-oxo-4-(phenyl-hydrazono)-4,5-dihydro-pyrazole-1-carbothioic acid phenylamide
CAS NO:78026-30-9
Molecular Formula:
Molecular Weight: 337.405
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-Methyl-5-oxo-4-(phenyl-hydrazono)-4,5-dihydro-pyrazole-1-carbothioic acid phenylamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-Methyl-5-oxo-4-(phenyl-hydrazono)-4,5-dihydro-pyrazole-1-carbothioic acid phenylamide(78026-30-9)
EPA Substance Registry System: 3-Methyl-5-oxo-4-(phenyl-hydrazono)-4,5-dihydro-pyrazole-1-carbothioic acid phenylamide(78026-30-9)

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: 78026-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78026-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,2 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78026-30:
(7*7)+(6*8)+(5*0)+(4*2)+(3*6)+(2*3)+(1*0)=129
129 % 10 = 9
So 78026-30-9 is a valid CAS Registry Number.

78026-30-9Upstream product

78026-30-9Downstream Products

78026-30-9Relevant academic research and scientific papers

Synthesis of some new phenylthiocarbamoyl 2-pyrazolin-5-ones of pharmaceutical interest

Metwally,Abdel-Latif,Amer

, p. 213 - 216 (2007/10/03)

Thiocarbamoylation reaction of 3-methyl-2-pyrazolin-5-one (1a) with two equivalents of PhNCS, resulted in the formation of 1,4-di(α-phenylthiocarbamoyl)-3-methylpyrazolone 3, which underwent cleavage of the thiocarbamoyl group at position 4 when coupled w

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