4388-06-1 Usage
Uses
Used in Pharmaceutical Applications:
In the pharmaceutical industry, [Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone,2,5'-dihydroxy-4,4'-dimethylcould be utilized as an active pharmaceutical ingredient (API) for the development of new drugs. Its unique structure may allow it to interact with specific biological targets, potentially leading to the creation of novel therapeutics.
Used in Organic Synthesis:
As an intermediate in organic synthesis, [Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone,2,5'-dihydroxy-4,4'-dimethylmay serve as a building block for the creation of more complex molecules. Its functional groups could be exploited in various chemical reactions, enabling the synthesis of a wide range of compounds with diverse applications.
Used in Material Sciences:
In the field of material sciences, [Bi-1,4-cyclohexadien-1-yl]-3,3',6,6'-tetrone,2,5'-dihydroxy-4,4'-dimethylmight be employed in the development of new materials with specific properties. Its structural features could contribute to the creation of materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 4388-06-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4388-06:
(6*4)+(5*3)+(4*8)+(3*8)+(2*0)+(1*6)=101
101 % 10 = 1
So 4388-06-1 is a valid CAS Registry Number.
4388-06-1Relevant academic research and scientific papers
An efficient synthesis of oosporein
Love, Brian E.,Bonner-Stewart, Jeffrey,Forrest, Lori A.
supporting information; experimental part, p. 5050 - 5052 (2009/12/05)
Fungal metabolite oosporein was prepared in four steps and 24% overall yield starting from 2,5-dimethoxytoluene. It was demonstrated that treatment of phoenicin with pyrrolidine and copper(II) acetate led to oosporein, whereas similar treatment of the isomeric 'isophoenicin' produced a benzofuran diquinone. No chromatography was required during any step of the synthesis.
