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Ethyl 3-(2-hydroxyphenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1491063-42-3 Structure
  • Basic information

    1. Product Name: Ethyl 3-(2-hydroxyphenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboxylate
    2. Synonyms: Ethyl 3-(2-hydroxyphenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboxylate
    3. CAS NO:1491063-42-3
    4. Molecular Formula:
    5. Molecular Weight: 340.379
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1491063-42-3.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: Ethyl 3-(2-hydroxyphenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethyl 3-(2-hydroxyphenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboxylate(1491063-42-3)
    11. EPA Substance Registry System: Ethyl 3-(2-hydroxyphenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboxylate(1491063-42-3)
  • 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: 1491063-42-3(Hazardous Substances Data)

1491063-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1491063-42-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,9,1,0,6 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1491063-42:
(9*1)+(8*4)+(7*9)+(6*1)+(5*0)+(4*6)+(3*3)+(2*4)+(1*2)=153
153 % 10 = 3
So 1491063-42-3 is a valid CAS Registry Number.

1491063-42-3Downstream Products

1491063-42-3Relevant articles and documents

Monoamine oxidase inhibitory activity of 3,5-biaryl-4,5-dihydro-1H- pyrazole-1-carboxylate derivatives

Vishnu Nayak,Ciftci-Yabanoglu,Jadav, Surender Singh,Jagrat, Monika,Sinha, Barij N.,Ucar,Jayaprakash, Venkatesan

, p. 762 - 767 (2013/10/22)

Ethyl and phenyl carbamate derivatives of pyrazoline (3a-3h) were synthesized and tested for their MAO inhibitory activity. All the compounds were found to be selective towards MAO-A. Phenyl carbamates (3e-3h) were better than ethyl carbamates (3a-3d) and

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