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602335-25-1

1H-Imidazole-1-propanoic acid, b-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 602335-25-1 Structure

  • Basic information

    1. Product Name: 1H-Imidazole-1-propanoic acid, b-phenyl-, ethyl ester
    2. Synonyms:
    3. CAS NO:602335-25-1
    4. Molecular Formula: C14H16N2O2
    5. Molecular Weight: 244.293
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 602335-25-1.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-Imidazole-1-propanoic acid, b-phenyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Imidazole-1-propanoic acid, b-phenyl-, ethyl ester(602335-25-1)
    11. EPA Substance Registry System: 1H-Imidazole-1-propanoic acid, b-phenyl-, ethyl ester(602335-25-1)

  • 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: 602335-25-1(Hazardous Substances Data)

602335-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 602335-25-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,2,3,3 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 602335-25:
(8*6)+(7*0)+(6*2)+(5*3)+(4*3)+(3*5)+(2*2)+(1*5)=111
111 % 10 = 1
So 602335-25-1 is a valid CAS Registry Number.

602335-25-1Downstream Products

602335-25-1Relevant articles and documents

Highly efficient and green chemical synthesis of imidazolyl alcohols and N-imidazolyl functionalized β-amino compounds using nanocrystalline ZSM-5 catalysts

Kore, Rajkumar,Satpati, Biswarup,Srivastava, Rajendra

, p. 8 - 17 (2014)

A solvent free protocol is developed for the synthesis of imidazolyl alcohols and N-imidazolyl functionalized β-amino compounds. Imidazolyl alcohols were synthesized by the ring opening of epoxides with imidazoles and N-imidazolyl functionalized β-amino compounds were synthesized by the hydroamination reaction of imidazoles and activated olefins. These reactions were catalyzed by a variety of crystalline heterogeneous catalysts such as Al/Zr substituted nanocrystalline ZSM-5 (M-Nano-ZSM-5), conventional M-ZSM-5 (where M = Zr, Al), and Zr substituted amorphous mesoporous catalysts (Zr-SBA-15 and Zr-KIT-6). Among these catalysts, nanocrystalline Zr-Nano-ZSM-5 exhibited the highest activity and regioselectivity. Structure activity relationship is explained based on the catalytic activity, acidity measurements, reactivity of reactants (imidazoles/epoxides/methyl acrylate), competitive adsorption, nature, and type of catalysts. Zr-Nano-ZSM-5 exhibited exceptionally high catalytic activity compared to the catalysts reported in the literature for the synthesis of imidazolyl alcohols and other imidazole derivatives.

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