Cas 132370-59-3,Ethanone, 2-(2,5-dihydro-1,2,2,5,5-pentamethyl-3-oxido-1H-imidazol-4-yl)-1-phen yl-, oxime

132370-59-3

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Basic information

Product Name: Ethanone, 2-(2,5-dihydro-1,2,2,5,5-pentamethyl-3-oxido-1H-imidazol-4-yl)-1-phen yl-, oxime
Synonyms:
CAS NO:132370-59-3
Molecular Formula: C16H23N3O2
Molecular Weight: 289.378
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: Ethanone, 2-(2,5-dihydro-1,2,2,5,5-pentamethyl-3-oxido-1H-imidazol-4-yl)-1-phen yl-, oxime(CAS DataBase Reference)
NIST Chemistry Reference: Ethanone, 2-(2,5-dihydro-1,2,2,5,5-pentamethyl-3-oxido-1H-imidazol-4-yl)-1-phen yl-, oxime(132370-59-3)
EPA Substance Registry System: Ethanone, 2-(2,5-dihydro-1,2,2,5,5-pentamethyl-3-oxido-1H-imidazol-4-yl)-1-phen yl-, oxime(132370-59-3)

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: 132370-59-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132370-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,7 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132370-59:
(8*1)+(7*3)+(6*2)+(5*3)+(4*7)+(3*0)+(2*5)+(1*9)=103
103 % 10 = 3
So 132370-59-3 is a valid CAS Registry Number.

132370-59-3Upstream product

129994-30-5 2-(1,2,2,5,5-Pentamethyl-3-oxy-2,5-dihydro-1H-imidazol-4-yl)-1-phenyl-ethanone

132370-59-3Downstream Products

132370-51-5 4-(1,2-dihydroximino-2-phenylethyl)-1,2,2,5,5-pentamethyl-3-imidazoline-3-oxide

132370-59-3Relevant academic research and scientific papers

REACTION OF β-OXONITRONES - IMIDAZOLINE AND PYRROLINE DERIVATIVES - WITH NUCLEOPHILIC REAGENTS

Reznikov, V. A.,Volodarski, L. B.

, p. 722 - 728 (1991)

The reaction of β-oxonitrones -imidazoline derivatives - with hydroxylamine, phenylhydrazine, and semicarbazide takes place at the carbonyl group with retention of the nitrone group.Stable nitroxyl radicals - spiroimidazoisoxazole derivatives - are formed

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