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1026926-22-6

N-(1-Benzyloxymethyl-5-bromo-3,4-dicyano-1H-pyrrol-2-yl)-formimidic acid 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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  • 1026926-22-6 Structure

  • Basic information

    1. Product Name: N-(1-Benzyloxymethyl-5-bromo-3,4-dicyano-1H-pyrrol-2-yl)-formimidic acid ethyl ester
    2. Synonyms: N-(1-Benzyloxymethyl-5-bromo-3,4-dicyano-1H-pyrrol-2-yl)-formimidic acid ethyl ester
    3. CAS NO:1026926-22-6
    4. Molecular Formula:
    5. Molecular Weight: 387.236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1026926-22-6.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: N-(1-Benzyloxymethyl-5-bromo-3,4-dicyano-1H-pyrrol-2-yl)-formimidic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-Benzyloxymethyl-5-bromo-3,4-dicyano-1H-pyrrol-2-yl)-formimidic acid ethyl ester(1026926-22-6)
    11. EPA Substance Registry System: N-(1-Benzyloxymethyl-5-bromo-3,4-dicyano-1H-pyrrol-2-yl)-formimidic acid ethyl ester(1026926-22-6)

  • 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: 1026926-22-6(Hazardous Substances Data)

1026926-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026926-22-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,9,2 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1026926-22:
(9*1)+(8*0)+(7*2)+(6*6)+(5*9)+(4*2)+(3*6)+(2*2)+(1*2)=136
136 % 10 = 6
So 1026926-22-6 is a valid CAS Registry Number.

1026926-22-6Relevant articles and documents

Synthesis of non-nucleoside analogs of toyocamycin, sangivamycin, and thiosangivamycin: Influence of various 7-substituents on antiviral activity

Renau, Thomas E.,Wotring, Linda L.,Drach, John C.,Townsend, Leroy B.

, p. 873 - 880 (1996)

A number of 7-substituted 4-aminopyrrolo[2,3-d]pyrimidine-5-carbonitrile, -5-carboxamide, and -5-thiocarboxamide derivatives related to the nucleoside antibiotics toyocamycin and sangivamycin were prepared and tested for their activity against human cytom

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