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201656-00-0

1H-Imidazole,1-(1-cyclopenten-1-yl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201656-00-0 Structure

  • Basic information

    1. Product Name: 1H-Imidazole,1-(1-cyclopenten-1-yl)-(9CI)
    2. Synonyms: 1H-Imidazole,1-(1-cyclopenten-1-yl)-(9CI)
    3. CAS NO:201656-00-0
    4. Molecular Formula: C8H10N2
    5. Molecular Weight: 134.1784
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 201656-00-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    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-(1-cyclopenten-1-yl)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Imidazole,1-(1-cyclopenten-1-yl)-(9CI)(201656-00-0)
    11. EPA Substance Registry System: 1H-Imidazole,1-(1-cyclopenten-1-yl)-(9CI)(201656-00-0)

  • 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: 201656-00-0(Hazardous Substances Data)

201656-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201656-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,6,5 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 201656-00:
(8*2)+(7*0)+(6*1)+(5*6)+(4*5)+(3*6)+(2*0)+(1*0)=90
90 % 10 = 0
So 201656-00-0 is a valid CAS Registry Number.

201656-00-0Upstream product

201656-00-0Downstream Products

201656-00-0Relevant articles and documents

Synthesis of N-cycloalkenylazoles.

Katritzky, Alan R,Maimait, Rexiat,Xu, Yong-Jiang,Gyoung, Young Soo

, p. 8230 - 8233 (2007/10/03)

N-(1-Cycloalkenyl)pyrroles 3a,b, -pyrazoles 6a,b, and -imidazoles 9a,b were synthesized via elimination of benzotriazole or 5-phenyltetrazole from the corresponding 1-[1-(heterocycyl)cycloalkyl]benzotriazoles 2, 5, and 8 or 1-[1-(heterocycyl)cyclohexyl]-5-phenyltetrazole (12 and 14). Intermediates 2, 5, 8, 12 and 14 were obtained by cyclizations of dihaloalkanes with N-(benzotriazol-1-ylmethyl)heterocycles, 1-imidazol-1-ylmethyl-5-phenyltetrazole (11), or 1-pyrazol-1-ylmethyl-5-phenyltetrazole (13) in the presence of n-BuLi.

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