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  • 1456928-83-8 Structure
  • Basic information

    1. Product Name: C20H14N2O3
    2. Synonyms:
    3. CAS NO:1456928-83-8
    4. Molecular Formula:
    5. Molecular Weight: 330.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1456928-83-8.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: C20H14N2O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H14N2O3(1456928-83-8)
    11. EPA Substance Registry System: C20H14N2O3(1456928-83-8)
  • 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: 1456928-83-8(Hazardous Substances Data)

1456928-83-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1456928-83-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,9,2 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1456928-83:
(9*1)+(8*4)+(7*5)+(6*6)+(5*9)+(4*2)+(3*8)+(2*8)+(1*3)=208
208 % 10 = 8
So 1456928-83-8 is a valid CAS Registry Number.

1456928-83-8Downstream Products

1456928-83-8Relevant articles and documents

Synthesis and antimicrobial screening of novel 3, 5-disubstituted indazole derivatives

Padmaja,Yedukondalu,Sridhar,Busi, Siddhardha,Rao, M.V. Basaveswara

, p. 625 - 631 (2013/08/23)

Amine coupling strategy was developed for the synthesis of new indazole derivatives through reaction of 4-(3- (4-hydroxyphenyl)-1-(tetrahydro-2H-pyran- 2-yl)-1H-indazol-5-yl) benzoic acid 19 with amines 20a-i. All the newly synthesized compounds were screened for their antimicrobial and antifungal activities. Among the several compounds synthesized (4-(3-(4-hydroxyphenyl)-1H- indol-5-yl)phenyl)(piperazin-1-yl)methanone 2, (4-(3-(4-hydroxyphenyl)- 1Hindazol- 5-yl)phenyl)(4-methylpiperazin-1-yl)methanone 3, 1-(4-(4-(3-(4- hydroxyphenyl)-1H-indol-5-yl) benzoyl) piperazin- 1-yl) ethanone 4 and (4-(3-(4-hydroxyphenyl)-1H-indol-5-yl) phenyl)(pyrrolidin-1-yl)methanone 9 showed potential activities against a variety of bacterial and fungal strains.

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