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113296-95-0

1H-Indol-1-yloxy, 5-[bis(4-methoxyphenyl)amino]-2,3-dihydro-3-oxo-2,2-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113296-95-0 Structure

  • Basic information

    1. Product Name: 1H-Indol-1-yloxy, 5-[bis(4-methoxyphenyl)amino]-2,3-dihydro-3-oxo-2,2-diphenyl-
    2. Synonyms:
    3. CAS NO:113296-95-0
    4. Molecular Formula: C34H27N2O4
    5. Molecular Weight: 527.599
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113296-95-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Indol-1-yloxy, 5-[bis(4-methoxyphenyl)amino]-2,3-dihydro-3-oxo-2,2-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indol-1-yloxy, 5-[bis(4-methoxyphenyl)amino]-2,3-dihydro-3-oxo-2,2-diphenyl-(113296-95-0)
    11. EPA Substance Registry System: 1H-Indol-1-yloxy, 5-[bis(4-methoxyphenyl)amino]-2,3-dihydro-3-oxo-2,2-diphenyl-(113296-95-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 113296-95-0(Hazardous Substances Data)

113296-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113296-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,9 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113296-95:
(8*1)+(7*1)+(6*3)+(5*2)+(4*9)+(3*6)+(2*9)+(1*5)=120
120 % 10 = 0
So 113296-95-0 is a valid CAS Registry Number.

113296-95-0Downstream Products

113296-95-0Relevant articles and documents

HOMOLYTIC SUBSTITUTION IN INDOLINONE NITROXIDES - IV. REACTIONS WITH AMINYL RADICALS. A SPECTROSCOPIC AND CRYSTALLOGRAPHIC STUDY.

Alberti, Angelo,Greci, Lucedio,Stipa, Pierluigi,Sgarabotto, Paolo,Ugozzoli, Franco

, p. 3031 - 3040 (2007/10/02)

The reactions between 2,2-diphenyl-indolinone-N-oxyl (3) and a series of aminyl radicals generated in situ by oxidation of secondary aromatic amines with PbO2 lead to aminated hydroxylamines (4), which in the presence of PbO2 are converted to the aminated nitroxides (5).When starting from primary amines, these are further oxidated to quinonimine-N-oxides (6) which then undergo nucleophilic substitution by another amine molecule to give the diaminated hydroxylamines (7).These are further oxidated to nitroxides (8), the final products of the reaction being the aminated quinone-diimine-N-oxides (9).The paramagnetic species (5) and (8) have been characterized using ESR spectroscopy; in addition, the molecular geometry of one of the N-oxides (9) was elucidated by means of X-ray structure analysis.

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