Cas 153787-24-7,4,5-Dimethyl-1,2-bis-(1,3,5-tri-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-1,2-dihydro-pyrazol-3-one

153787-24-7

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Basic information

Product Name: 4,5-Dimethyl-1,2-bis-(1,3,5-tri-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-1,2-dihydro-pyrazol-3-one
Synonyms: 4,5-Dimethyl-1,2-bis-(1,3,5-tri-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-1,2-dihydro-pyrazol-3-one
CAS NO:153787-24-7
Molecular Formula:
Molecular Weight: 632.971
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: 4,5-Dimethyl-1,2-bis-(1,3,5-tri-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-1,2-dihydro-pyrazol-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 4,5-Dimethyl-1,2-bis-(1,3,5-tri-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-1,2-dihydro-pyrazol-3-one(153787-24-7)
EPA Substance Registry System: 4,5-Dimethyl-1,2-bis-(1,3,5-tri-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-1,2-dihydro-pyrazol-3-one(153787-24-7)

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: 153787-24-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 153787-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,7,8 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153787-24:
(8*1)+(7*5)+(6*3)+(5*7)+(4*8)+(3*7)+(2*2)+(1*4)=157
157 % 10 = 7
So 153787-24-7 is a valid CAS Registry Number.

153787-24-7Upstream product

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153787-24-7Relevant academic research and scientific papers

Free Radical Reactions of N-Heterocyclic Compounds. XI. Reaction of 3-Methyl-pyrazolin-5-ones with Phenoxy Radicals

Schulz, Manfred,Meske, Michael

, p. 607 - 615 (2007/10/02)

Pyrazolin-5-ones (3a-i) were oxidized with 2,4,6-trisubstituted phenoxy radicals (2a-d) to the corresponding radicals (4a-i), which dimerised or combined with phenoxy radical (2a) depending on the R1- and R4-substituents in (3).In th

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