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264121-82-6

2,3-bis[(4-methoxy-2-formylphenoxy)methyl]quinoxaline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 264121-82-6 Structure

  • Basic information

    1. Product Name: 2,3-bis[(4-methoxy-2-formylphenoxy)methyl]quinoxaline
    2. Synonyms:
    3. CAS NO:264121-82-6
    4. Molecular Formula:
    5. Molecular Weight: 458.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 264121-82-6.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: 2,3-bis[(4-methoxy-2-formylphenoxy)methyl]quinoxaline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-bis[(4-methoxy-2-formylphenoxy)methyl]quinoxaline(264121-82-6)
    11. EPA Substance Registry System: 2,3-bis[(4-methoxy-2-formylphenoxy)methyl]quinoxaline(264121-82-6)

  • 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: 264121-82-6(Hazardous Substances Data)

264121-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 264121-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,1,2 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 264121-82:
(8*2)+(7*6)+(6*4)+(5*1)+(4*2)+(3*1)+(2*8)+(1*2)=116
116 % 10 = 6
So 264121-82-6 is a valid CAS Registry Number.

264121-82-6Downstream Products

264121-82-6Relevant articles and documents

Synthesis of new benzo-substituted macrocyclic ligands containing quinoxaline subunits

Elwahy, Ahmed H. M.

, p. 897 - 907 (2007/10/03)

The macrocyclic Schiff bases 20-25 were prepared by cyclocondensation of the bis aldehydes 12-15 with the appropriate diaminoalkanes 17-19. Reduction of the latter with NaBH4 afforded the corresponding azacrown ethers 27-30. Heating of the aldehydes 12-16 in refluxing acetic acid afforded the corresponding 2,3-bis(benzofuranyl)quinoxalines 33-37. Nucleophilic reaction of the bis phenols 45-48, 54, 56, 57 with the appropriate dihalo compounds 1, 38 afforded the corresponding macrocyclic diamides 49-52 and 1,ω- bis[quinoxalino(2,3-b)benzoxazepino-13-on-yl]alkanes 60, 61, respectively. (C) 2000 Elsevier Science Ltd.

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