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214633-81-5

Ethanone, 1-(4-methylphenyl)-2-[3-(4-methylphenyl)-2(1H)-quinoxalinylidene]-, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214633-81-5 Structure

  • Basic information

    1. Product Name: Ethanone, 1-(4-methylphenyl)-2-[3-(4-methylphenyl)-2(1H)-quinoxalinylidene]-, (2Z)-
    2. Synonyms:
    3. CAS NO:214633-81-5
    4. Molecular Formula: C24H20N2O
    5. Molecular Weight: 352.436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214633-81-5.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: Ethanone, 1-(4-methylphenyl)-2-[3-(4-methylphenyl)-2(1H)-quinoxalinylidene]-, (2Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(4-methylphenyl)-2-[3-(4-methylphenyl)-2(1H)-quinoxalinylidene]-, (2Z)-(214633-81-5)
    11. EPA Substance Registry System: Ethanone, 1-(4-methylphenyl)-2-[3-(4-methylphenyl)-2(1H)-quinoxalinylidene]-, (2Z)-(214633-81-5)

  • 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: 214633-81-5(Hazardous Substances Data)

214633-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214633-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,6,3 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 214633-81:
(8*2)+(7*1)+(6*4)+(5*6)+(4*3)+(3*3)+(2*8)+(1*1)=115
115 % 10 = 5
So 214633-81-5 is a valid CAS Registry Number.

214633-81-5Relevant articles and documents

Opening of the Furandione Ring with o-Aminothiophenol: Synthesis of 2H-1,4-Benzothiazine-2,3(4H)-dione

Tretyakov,Dmitriev,Shein,Maslivets

, p. 716 - 718 (2019)

5-Aryl-4-(3-arylquinoxalin-2-yl)furan-2,3-diones react with o-aminothiophenol to form 2H-1,4-benzothiazin-2,3-(4H)-dione and (2Z)-1-aryl-2-[3-arylquinoxalin-2(1H)-ylidene]ethan-1-ones.

A new route to construct 1,2-dihydroquinoxaline and 1,4-benzoxazine derivatives stereoselectively and its application to novel pyrazolo[1,5-α] quinoxaline oxides

Zhang, Dongxue,Yang, Yan,Gao, Meng,Shu, Wenming,Wu, Liuming,Zhu, Yanping,Wu, Anxin

supporting information, p. 1849 - 1856 (2013/04/23)

1,2-Dihydroquinoxaline and 1,4-benzoxazine skeletons were constructed stereoselectively from easily available aryl methyl ketones via a two-step procedure in mild conditions with high yields. Moreover, the application of this reaction provided a convenien

Efficient synthesis of dialkyl (2Z)-2-[(E)-1-aryl-2-(3-arylquinoxalin-2-yl) ethenyl]but-2-enedioates

Yavari, Issa,Mirzaei, Anvar,Moradi, Loghman

, p. 2825 - 2829 (2007/10/03)

The reaction of dialkyl acetylenedicarboxylates 4 with 1-aryl-2-[(3- arylquinoxalin-2(1H)-ylidene)-ethanones 3 in the presence of Ph3P leads to dialkyl (2Z)-2-[(E)-1-aryl-2-(3-arylquinoxalin-2-yl)ethenyl]-but-2- enedioates 1 in good yields.

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