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CAS

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88235-71-6

2-Imidazolidinone, 5-(hydroxyamino)-3,4,4-trimethyl-1-(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88235-71-6 Structure

  • Basic information

    1. Product Name: 2-Imidazolidinone, 5-(hydroxyamino)-3,4,4-trimethyl-1-(1-phenylethyl)-
    2. Synonyms:
    3. CAS NO:88235-71-6
    4. Molecular Formula: C14H21N3O2
    5. Molecular Weight: 263.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88235-71-6.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: 2-Imidazolidinone, 5-(hydroxyamino)-3,4,4-trimethyl-1-(1-phenylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Imidazolidinone, 5-(hydroxyamino)-3,4,4-trimethyl-1-(1-phenylethyl)-(88235-71-6)
    11. EPA Substance Registry System: 2-Imidazolidinone, 5-(hydroxyamino)-3,4,4-trimethyl-1-(1-phenylethyl)-(88235-71-6)

  • 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: 88235-71-6(Hazardous Substances Data)

88235-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88235-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88235-71:
(7*8)+(6*8)+(5*2)+(4*3)+(3*5)+(2*7)+(1*1)=156
156 % 10 = 6
So 88235-71-6 is a valid CAS Registry Number.

88235-71-6Relevant articles and documents

OXIDATION AND REDUCTION OF SUBSTITUTED 4-HYDROXYAMINO AND 4-OXIMINOIMIDAZOLIDIN-2-ONES

Epshtein, S. P.,Rukasov, A. F.,Tashchi, V. P.,Simonova, T. G.,Putsykin, Yu. G.

, p. 993 - 996 (1983)

4-Oximino-3-aryl(alkyl)-5,5-dimethylimidazolidin-2-ones were obtained by air oxidation of substituted 4-hydroxyaminoimidazolidin-2-ones in the presence of sodium ethoxide.In hydrochloric acid 4-oximino-3-(3',4'-dichlorophenyl)imidazolidin-2-one gives the corresponding hydantoin, whereas 4-oximino-3-(1'-phenylethyl)imidazolidin-2-one gives its E isomer with respect to the oxime group.The reduction of 4-oximino-3-alkylimidazolidin-2-ones with Raney alloy in 20percent NaOH or hydrogenation on a palladium catalyst leads to 4-imino derivatives, whereas reduction of 4-oximino-3-aryl-5,5-dimethylimidazolidin-2-ones that contain chlorine atoms in their aromatic rings with sodium in liquid ammonia leads to their dehalogenation.

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