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131706-04-2

2-phenyl-6-methoxyquinoxaline 4-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131706-04-2 Structure

  • Basic information

    1. Product Name: 2-phenyl-6-methoxyquinoxaline 4-oxide
    2. Synonyms: 2-phenyl-6-methoxyquinoxaline 4-oxide
    3. CAS NO:131706-04-2
    4. Molecular Formula:
    5. Molecular Weight: 252.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131706-04-2.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: 2-phenyl-6-methoxyquinoxaline 4-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenyl-6-methoxyquinoxaline 4-oxide(131706-04-2)
    11. EPA Substance Registry System: 2-phenyl-6-methoxyquinoxaline 4-oxide(131706-04-2)

  • 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: 131706-04-2(Hazardous Substances Data)

131706-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131706-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,0 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131706-04:
(8*1)+(7*3)+(6*1)+(5*7)+(4*0)+(3*6)+(2*0)+(1*4)=92
92 % 10 = 2
So 131706-04-2 is a valid CAS Registry Number.

131706-04-2Relevant articles and documents

Dehydrogenative N-incorporation: A direct approach to quinoxaline N-oxides under mild conditions

Chen, Feng,Huang, Xiaoqiang,Li, Xinyao,Shen, Tao,Zou, Miancheng,Jiao, Ning

, p. 10495 - 10499 (2014)

An efficient method for the synthesis of quinoxaline N-oxides proceeds by the dehydrogenative N-incorporation of simple imines by C(sp2)-H and C(sp3)-H bond functionalization. The overall transformation involves the cleavage of three

2-Phenyl-(6(7)-R-substituted quinoxalines N-oxides. Synthesis, structure elucidation and antimicrobial activity

Loriga,Nuvole,Paglietti,Fadda,Zanetti

, p. 527 - 532 (2007/10/02)

A certain number of isomeric 2-phenylquinoxalines N-oxides bearing substituents at position 6/7 were prepared in order to investigate anti-microbial activity. The effect of some electron-withdrawing groups seem to increase an anti-Trichomonas vaginalis ac

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