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1-(3-hydroxy-1-methyl-2-butenylideneamino)benzimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 261710-15-0 Structure
  • Basic information

    1. Product Name: 1-(3-hydroxy-1-methyl-2-butenylideneamino)benzimidazole
    2. Synonyms:
    3. CAS NO:261710-15-0
    4. Molecular Formula:
    5. Molecular Weight: 215.255
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 261710-15-0.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: 1-(3-hydroxy-1-methyl-2-butenylideneamino)benzimidazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3-hydroxy-1-methyl-2-butenylideneamino)benzimidazole(261710-15-0)
    11. EPA Substance Registry System: 1-(3-hydroxy-1-methyl-2-butenylideneamino)benzimidazole(261710-15-0)
  • 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: 261710-15-0(Hazardous Substances Data)

261710-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261710-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,7,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 261710-15:
(8*2)+(7*6)+(6*1)+(5*7)+(4*1)+(3*0)+(2*1)+(1*5)=110
110 % 10 = 0
So 261710-15-0 is a valid CAS Registry Number.

261710-15-0Relevant articles and documents

Reactions of a series of 1-aminobenzimidazoles and 1-amino-3- methylbenzimidazolium chlorides with 2,4-pentanedione

Kaiya, Toyo,Aoyama, Shinsuke,Kohda, Kohfuku

, p. 37 - 42 (2000)

Reactions of a series of 1-aminobenzimidazoles and 1-amino-3- methylbenzimidazolium chlorides with 2,4-pentanedione were carried out and pyridazino[1,6-a]benzimidazoles and 2-pyrazolylanilines were generated. The product ratios of these compounds remarkably depended on the reaction conditions and on the electronic character of the substituent at the benzene moiety. The possible mechanisms involved in these reactions are discussed. (C) 2000 Elsevier Science Ltd.

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