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145083-30-3

(1-Benzyl-2-methylsulfanyl-1H-imidazol-4-yl)-phenyl-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145083-30-3 Structure

  • Basic information

    1. Product Name: (1-Benzyl-2-methylsulfanyl-1H-imidazol-4-yl)-phenyl-methanol
    2. Synonyms:
    3. CAS NO:145083-30-3
    4. Molecular Formula:
    5. Molecular Weight: 310.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145083-30-3.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-Benzyl-2-methylsulfanyl-1H-imidazol-4-yl)-phenyl-methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1-Benzyl-2-methylsulfanyl-1H-imidazol-4-yl)-phenyl-methanol(145083-30-3)
    11. EPA Substance Registry System: (1-Benzyl-2-methylsulfanyl-1H-imidazol-4-yl)-phenyl-methanol(145083-30-3)

  • 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: 145083-30-3(Hazardous Substances Data)

145083-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145083-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,8 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 145083-30:
(8*1)+(7*4)+(6*5)+(5*0)+(4*8)+(3*3)+(2*3)+(1*0)=113
113 % 10 = 3
So 145083-30-3 is a valid CAS Registry Number.

145083-30-3Downstream Products

145083-30-3Relevant articles and documents

Single-flask polyfunctionalization of the imidazole ring; a streamlined route to the antitumor agent carmethizole

Lipshutz, Bruce H.,Hagen, William

, p. 5865 - 5868 (1992)

Three sequential treatments of an N-protected tribromoimidazole with n-BuLi/electrophile in a 1-pot process leads to N-protected 2,4,5-trisubstituted imidazoles. The method can be applied to the preparation of the immediate of carmethizole.

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