Welcome to LookChem.com Sign In|Join Free
  • or
4,6-di-tert-butyl-8-methoxydibenzofuran-1,2-quinone is a complex organic compound characterized by its unique molecular structure. It belongs to the class of dibenzofuran-quinones, which are known for their diverse applications in chemical research and pharmaceuticals. This particular compound is distinguished by the presence of two tert-butyl groups at the 4 and 6 positions, which contribute to its stability and reactivity, and a methoxy group at the 8 position, which influences its electronic properties. The compound's quinone moiety, consisting of a 1,2-quinone structure, is central to its redox properties and potential involvement in electron transfer reactions. Overall, 4,6-di-tert-butyl-8-methoxydibenzofuran-1,2-quinone is a synthetically interesting and potentially useful molecule in the field of organic chemistry, with potential applications in the development of new materials and pharmaceuticals.

4950-32-7

Post Buying Request

4950-32-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4950-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4950-32-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,5 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4950-32:
(6*4)+(5*9)+(4*5)+(3*0)+(2*3)+(1*2)=97
97 % 10 = 7
So 4950-32-7 is a valid CAS Registry Number.

4950-32-7Downstream Products

4950-32-7Relevant academic research and scientific papers

Oxidation of Alkoxyphenols. XXIX Phototautomerism and Dimerization of 4,6-Di-t-butyl-4a-hydroxy-8-methoxydibenzofuran-2(4aH)-one

Hewgill, Frank R.,Raston, Colin L.,Skelton, Brian W.,Webb, Rauleigh J.,White, Allan H.

, p. 1603 - 1614 (2007/10/02)

In solution in no-polar solvents the title compound undergoes photochemical ring opening to its hydroxyphenylquinone tautomer.Oxidation of 3,3'-di-t-butyl-5,5'-dimethoxybiphenyl-2,2'-diol with vanadium oxytrifluoride in the presence of trifluoroacetic aci

Oxidative Conversions of 2,2'-Diphenoquinone Valence Isomers with 2,3-Dichloro-5,6-dicyanobenzoquinone. Synthesis and Spectroscopic Properties of (E)-Bibenzofuranylidene-2,2'-diones (Isoxindigos)

Becker, Hans-Dieter,Lingnert, Hans

, p. 1095 - 1101 (2007/10/02)

Oxepinobenzofurans derived from tetraalkyl-substituted and dialkyldimethoxy-substituted 2,2'-diphenoquinones by spontaneous valence isomerization react with 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) in the presence of water to give benzofuranyliden-2-one

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 4950-32-7