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2-(4-Methoxy-3,5-dimethyl-phenyl)-furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156360-13-3 Structure
  • Basic information

    1. Product Name: 2-(4-Methoxy-3,5-dimethyl-phenyl)-furan
    2. Synonyms:
    3. CAS NO:156360-13-3
    4. Molecular Formula:
    5. Molecular Weight: 202.253
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156360-13-3.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: 2-(4-Methoxy-3,5-dimethyl-phenyl)-furan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-Methoxy-3,5-dimethyl-phenyl)-furan(156360-13-3)
    11. EPA Substance Registry System: 2-(4-Methoxy-3,5-dimethyl-phenyl)-furan(156360-13-3)
  • 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: 156360-13-3(Hazardous Substances Data)

156360-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156360-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,6 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156360-13:
(8*1)+(7*5)+(6*6)+(5*3)+(4*6)+(3*0)+(2*1)+(1*3)=123
123 % 10 = 3
So 156360-13-3 is a valid CAS Registry Number.

156360-13-3Relevant articles and documents

Novel Amphoteric 2,5-Furoquinonoid-Containing p-Terphenoquinone Analogues Giving Both a Stable Radical Anion and a Stable Radical Cation

Takahashi, Kazuko,Gunji, Atsushi,Akiyama, Kimio

, p. 863 - 866 (1994)

Novel p-terphenoquinone analogues incorporating a central dihydrofurandiylidene skeleton have been synthesized.These quinones gave a stable radical kation and a stable radical anion on one-electron redox reactions showing an amphoteric property even though they do not contain any sulfur atom as an integral component.The radical cation and the radical anion of the tetra-t-butyl derivative have been characterized by EPR spectroscopy.

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