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CAS

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88100-22-5

1H-Imidazole-4-carboxamide, 5-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88100-22-5 Structure

  • Basic information

    1. Product Name: 1H-Imidazole-4-carboxamide, 5-(phenylmethoxy)-
    2. Synonyms:
    3. CAS NO:88100-22-5
    4. Molecular Formula: C11H11N3O2
    5. Molecular Weight: 217.227
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88100-22-5.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-4-carboxamide, 5-(phenylmethoxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Imidazole-4-carboxamide, 5-(phenylmethoxy)-(88100-22-5)
    11. EPA Substance Registry System: 1H-Imidazole-4-carboxamide, 5-(phenylmethoxy)-(88100-22-5)

  • 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: 88100-22-5(Hazardous Substances Data)

88100-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88100-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,0 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88100-22:
(7*8)+(6*8)+(5*1)+(4*0)+(3*0)+(2*2)+(1*2)=115
115 % 10 = 5
So 88100-22-5 is a valid CAS Registry Number.

88100-22-5Downstream Products

88100-22-5Relevant articles and documents

Studies on imidazole derivatives and related compounds. II. Characterization of substituted derivatives of 4-carbamoylimidazolium-5-olate by ultraviolet absorption spectra

Tarumi,Atsumi

, p. 875 - 885 (1983)

The representative mono- and dialkyl-substituted derivatives of 4-carbamoylimidazolium-5-olate were synthesized unequivocally. On the basis of their spectral data from ultraviolet absorption spectra in acidic, basic and neutral solutions, we have found so

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