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CAS

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244246-34-2

Phenyl-(1-methyl-5-phenyl-1H-pyrazol-4-yl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 244246-34-2 Structure

  • Basic information

    1. Product Name: Phenyl-(1-methyl-5-phenyl-1H-pyrazol-4-yl)methanol
    2. Synonyms:
    3. CAS NO:244246-34-2
    4. Molecular Formula:
    5. Molecular Weight: 264.327
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 244246-34-2.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: Phenyl-(1-methyl-5-phenyl-1H-pyrazol-4-yl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenyl-(1-methyl-5-phenyl-1H-pyrazol-4-yl)methanol(244246-34-2)
    11. EPA Substance Registry System: Phenyl-(1-methyl-5-phenyl-1H-pyrazol-4-yl)methanol(244246-34-2)

  • 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: 244246-34-2(Hazardous Substances Data)

244246-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244246-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,2,4 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 244246-34:
(8*2)+(7*4)+(6*4)+(5*2)+(4*4)+(3*6)+(2*3)+(1*4)=122
122 % 10 = 2
So 244246-34-2 is a valid CAS Registry Number.

244246-34-2Downstream Products

244246-34-2Relevant articles and documents

Synthesis and biological evaluation of [α-(1,5-disubstituted 1H-pyrazol-4-yl)benzyl]azoles, analogues of bifonazole

Menozzi, Giulia,Mosti, Luisa,Bruno, Olga,Lo Presti, Eleonora,Musiu, Chiara,Longu, Silvia,La Colla, Paolo,Filippelli, Walter,Falcone, Giuseppe,Piucci, Brunella

, p. 416 - 422 (1999)

A series of pyrazole analogues of bifonazole, an antifungal drug used in clinical practice, 2a-h and 4a-h were synthesized and tested in vitro against Candida albicans, Cryptococcus neoformans and Aspergillus fumigatus, with no significant results. Imidazoles 2a-h were also tested in vivo for antiarrhythmic and antihypertensive activities; two of these compounds showed moderate activity against ventricular fibrillation caused by aconitine in rats. The above compounds were prepared by reaction of phenyl-[5 substituted 1-phenyl (or 1-methyl)-1H-pyrazol-4-yl]methanols with N,N'-carbonyldiimidazole (2a-h) or of the respective chloro derivatives with 1H-1,2,4-triazole (4a-h).

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