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359792-99-7

2-azido-1-benzyloxymethylimidazo[4,5-b]pyrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 359792-99-7 Structure

  • Basic information

    1. Product Name: 2-azido-1-benzyloxymethylimidazo[4,5-b]pyrazine
    2. Synonyms: 2-azido-1-benzyloxymethylimidazo[4,5-b]pyrazine
    3. CAS NO:359792-99-7
    4. Molecular Formula:
    5. Molecular Weight: 281.277
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 359792-99-7.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-azido-1-benzyloxymethylimidazo[4,5-b]pyrazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-azido-1-benzyloxymethylimidazo[4,5-b]pyrazine(359792-99-7)
    11. EPA Substance Registry System: 2-azido-1-benzyloxymethylimidazo[4,5-b]pyrazine(359792-99-7)

  • 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: 359792-99-7(Hazardous Substances Data)

359792-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359792-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,7,9 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 359792-99:
(8*3)+(7*5)+(6*9)+(5*7)+(4*9)+(3*2)+(2*9)+(1*9)=217
217 % 10 = 7
So 359792-99-7 is a valid CAS Registry Number.

359792-99-7Relevant articles and documents

Dienophilicity of imidazole in inverse electron demand Diels-Alder reactions: Cycloadditions with 1,2,4,5-tetrazines and the structure of zarzissine

Wan, Zhao-Kui,Woo, Grace H.C.,Snyder, John K.

, p. 5497 - 5507 (2007/10/03)

The inverse electron demand cycloadditions of 2-substituted imidazoles with dimethyl 1,2,4,5-tetrazine-3,6-dicarboxylate produced imidazo[4,5-d]pyridazines in good yields. This chemistry was applied to the synthesis of 2-amino-1H-imidazo[4,5-d]pyridazine (1), the structure reported for zarzissine, a cytotoxic marine alkaloid. Differences in the 1H- and 13C NMR spectra of 1 with those reported for zarzissine necessitated a structural revision, and zarzissine was then considered to be the corresponding 2-amino-1H-imidazo[4,5-b]pyrazine (2), which was subsequently synthesized from the parent heterocycle.

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