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C19H20O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1018466-23-3 Structure
  • Basic information

    1. Product Name: C19H20O2
    2. Synonyms: C19H20O2
    3. CAS NO:1018466-23-3
    4. Molecular Formula:
    5. Molecular Weight: 280.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1018466-23-3.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: C19H20O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H20O2(1018466-23-3)
    11. EPA Substance Registry System: C19H20O2(1018466-23-3)
  • 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: 1018466-23-3(Hazardous Substances Data)

1018466-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1018466-23-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,4,6 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1018466-23:
(9*1)+(8*0)+(7*1)+(6*8)+(5*4)+(4*6)+(3*6)+(2*2)+(1*3)=133
133 % 10 = 3
So 1018466-23-3 is a valid CAS Registry Number.

1018466-23-3Downstream Products

1018466-23-3Relevant articles and documents

Synthesis and antimicrobial activity of some novel derivatives of benzofuran: Part 2. The synthesis and antimicrobial activity of some novel 1-(1-benzofuran-2-yl)-2-mesitylethanone derivatives

Kirilmis, Cumhur,Ahmedzade, Misir,Servi, Sueleyman,Koca, Murat,Kizirgil, Ahmet,Kazaz, Cavit

, p. 300 - 308 (2008/09/18)

The reaction of salicylaldehyde with 1-chloro-3-mesitylacetone (2) and potassium carbonate was used to prepare 1-(1-benzofuran-2-yl)-2-mesitylethanone (4) for the starting reagent purposes. 1-(1-Benzofuran-2-yl)-2-mesitylethanoneoxime (5) was synthesized by the reaction of the compound (4) with hydroxylamine. New derivative of 1-(1-benzofuran-2-yl)-2-mesitylethanoneoxime (5) as 1-(1-benzofuran-2-yl)-2-mesitylethanonesemicarbazone (7) was obtained in very high yields. Alkyl substituted N-oxime ethers (8a-d) were obtained by the reaction compound 5 and various halogen contained compounds. The compounds 9a-d were synthesized by the reaction of the compound (5) and four different acyl chlorides. Some of the synthesized compounds were tested for antimicrobial activity against Staphylococcus aureus ATCC 6538, Escherichia coli ATCC 25922 and Candida albicans ATCC 10231. Among the synthesized compounds (E)-1-(1-benzofuran-2-yl)-2-mesitylethanone-O-benzoyloxime (9b) was found the most active derivative against S. aureus ATCC 6538 and E. coli ATCC 25922. The other compounds exhibited moderate activity against the other test microorganisms.

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