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4-butyl-7,8-dimethoxy-3-phenylnaphtho[2,1-d]isoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1440337-93-8 Structure
  • Basic information

    1. Product Name: 4-butyl-7,8-dimethoxy-3-phenylnaphtho[2,1-d]isoxazole
    2. Synonyms:
    3. CAS NO:1440337-93-8
    4. Molecular Formula:
    5. Molecular Weight: 361.441
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1440337-93-8.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: 4-butyl-7,8-dimethoxy-3-phenylnaphtho[2,1-d]isoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-butyl-7,8-dimethoxy-3-phenylnaphtho[2,1-d]isoxazole(1440337-93-8)
    11. EPA Substance Registry System: 4-butyl-7,8-dimethoxy-3-phenylnaphtho[2,1-d]isoxazole(1440337-93-8)
  • 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: 1440337-93-8(Hazardous Substances Data)

1440337-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440337-93-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,3,3 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1440337-93:
(9*1)+(8*4)+(7*4)+(6*0)+(5*3)+(4*3)+(3*7)+(2*9)+(1*3)=138
138 % 10 = 8
So 1440337-93-8 is a valid CAS Registry Number.

1440337-93-8Upstream product

1440337-93-8Downstream Products

1440337-93-8Relevant articles and documents

A tandem strategy for the synthesis of 1H-benzo[g]indazoles and naphtho[2,1-d]isoxazoles from o-alkynylarene chalcones

Akbar, Sikkandarkani,Srinivasan, Kannupal

, p. 1663 - 1666 (2013)

o-Alkynylarene chalcones when treated with hydrazines and hydroxylamine in the presence of iodine gave 1H-benzo[g]indazoles and naphtho[2,1-d]isoxazoles, respectively. The transformations involve tandem oxidative cyclocondensation/ electrophilic hydroarylation. The methodology was applied to quinoline-based chalcones, which also afforded the corresponding quinoline-fused benzindazole and benzisoxazole. o-Alkynylarene chalcones undergo tandem oxidative cyclocondensation/electrophilic hydroarylation with arylhydrazines and hydroxylamine in the presence of iodine to afford 1H-benzo[g]indazoles and naphtho[2,1-d]isoxazoles, respectively. Copyright

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