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1H-Pyrazole-3-carboxamide, 4-benzoyl-1,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 188724-67-6 Structure
  • Basic information

    1. Product Name: 1H-Pyrazole-3-carboxamide, 4-benzoyl-1,5-diphenyl-
    2. Synonyms:
    3. CAS NO:188724-67-6
    4. Molecular Formula: C23H17N3O2
    5. Molecular Weight: 367.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 188724-67-6.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: 1H-Pyrazole-3-carboxamide, 4-benzoyl-1,5-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrazole-3-carboxamide, 4-benzoyl-1,5-diphenyl-(188724-67-6)
    11. EPA Substance Registry System: 1H-Pyrazole-3-carboxamide, 4-benzoyl-1,5-diphenyl-(188724-67-6)
  • 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: 188724-67-6(Hazardous Substances Data)

188724-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188724-67-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,2 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 188724-67:
(8*1)+(7*8)+(6*8)+(5*7)+(4*2)+(3*4)+(2*6)+(1*7)=186
186 % 10 = 6
So 188724-67-6 is a valid CAS Registry Number.

188724-67-6Relevant articles and documents

Functionalization and Cyclization Reactions of 4-Benzoyl-1,5-diphenyl- 1H-pyrazole-3-carboxylic Acid

Akcamur, Yunus,Sener, Ahmet,Ipekoglu, Alemdar Mustafa,Kollenz, Gert

, p. 221 - 224 (2007/10/03)

The 1H-pyrazole-3-carboxylic acid 2 or its remarkably stable acid chloride 3 can easily be converted into the corresponding ester or amide derivatives 4 or 5, respectively, from reaction with alcohols or N-nucleophiles. Pyrazolo[3,4-d]pyridazines 6a,b are obtained from cyclocondensation reactions of the pyrazoles 2 and 3, respectively, with phenylhydrazine or hydrazine hydrate, while 6c is formed in an one-pot procedure from the furan-2,3-dione 1 and hydrazine hydrate.

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