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CAS

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92764-06-2

Imidazolidinetrione, (3-phenylpropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92764-06-2 Structure

  • Basic information

    1. Product Name: Imidazolidinetrione, (3-phenylpropyl)-
    2. Synonyms:
    3. CAS NO:92764-06-2
    4. Molecular Formula: C12H12N2O3
    5. Molecular Weight: 232.239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92764-06-2.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: Imidazolidinetrione, (3-phenylpropyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Imidazolidinetrione, (3-phenylpropyl)-(92764-06-2)
    11. EPA Substance Registry System: Imidazolidinetrione, (3-phenylpropyl)-(92764-06-2)

  • 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: 92764-06-2(Hazardous Substances Data)

92764-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92764-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,6 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92764-06:
(7*9)+(6*2)+(5*7)+(4*6)+(3*4)+(2*0)+(1*6)=152
152 % 10 = 2
So 92764-06-2 is a valid CAS Registry Number.

92764-06-2Relevant articles and documents

Highly selective aldose reductase inhibitors. 1. 3-(Arylalkyl)-2,4,5- trioxoimidazolidine-1-acetic acids

Ishii,Kotani,Nagaki,Shibayama,Toyomaki,Okukado,Ienaga,Okamoto

, p. 1924 - 1927 (2007/10/03)

A series of 3-(arylalkyl)-2,4,5-trioxoimidazolidine-1-acetic acids (1) was prepared and tested for aldose reductase (AR) and aldehyde reductase (ALR) inhibitory activities. These compounds showed strong inhibitory activity against AR without significant inhibitory activity for ALR. The ratio of IC50(ALR)IC50(AR) was > 1000 in some compounds. On the basis of pharmacological tests such as the recovery of reduced motor nerve conduction velocity and toxicological profile, 3-(3-nitrobenzyl)-2,4,5- trioxoimidazolidine-1-acetic acid (NZ-314) was selected as the candidate for clinical development.

Synthesis of Substituted 2-Imidazolidinones and Annelated Hydantions via Aminoalkylation Transformations

Liao, Zeng-Kun,Kohn, Harold

, p. 4745 - 4752 (2007/10/02)

The synthetic utility of 4-hydroxy-2-imidazolidinone amidoalkylation reactions is limited by the propensity of the carbon-5 unsubstituted and carbon-5 monosubstituted adducts to undergo dehydration to yield 2-imidazolones.Two techniques are reported which

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