4388-07-2 Usage
Uses
Used in Organic Chemistry:
4,4'-Dimethyl-1,1'-biphenyl-2,2',5,5'-tetraone is used as a building block for the synthesis of other organic compounds due to its unique molecular structure and reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4'-Dimethyl-1,1'-biphenyl-2,2',5,5'-tetraone is used as a reactant in chemical reactions to create new pharmaceutical compounds, contributing to the development of novel drugs.
Used in Materials Science:
4,4'-Dimethyl-1,1'-biphenyl-2,2',5,5'-tetraone is utilized in materials science for its potential applications in creating new materials with specific properties, such as high thermal stability or unique optical characteristics.
Used in Chemical Synthesis:
As a reactant in chemical synthesis, 4,4'-Dimethyl-1,1'-biphenyl-2,2',5,5'-tetraone is employed to produce a variety of chemical products, taking advantage of its reactivity and structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 4388-07-2 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 4388-07:
(6*4)+(5*3)+(4*8)+(3*8)+(2*0)+(1*7)=102
102 % 10 = 2
So 4388-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H22N6O3S/c1-13-4-7-15(8-5-13)24-19(29)11-18-20(30)25-21(32-18)26-23-12-14-6-9-16-17(10-14)28(3)22(31)27(16)2/h4-10,12,18H,11H2,1-3H3,(H,24,29)(H,25,26,30)
4388-07-2Relevant academic research and scientific papers
Substituent effects in the oxidation of 2-alkyl-1,4-dialkoxybenzenes with ceric ammonium nitrate
Love, Brian E.,Simmons, Alexander L.
, p. 5712 - 5715 (2016/11/29)
Increased steric size of alkyl groups and the presence of coordinating atoms on alkoxy groups have both been found to contribute to decreasing yields of diquinones upon reaction of 2-alkyl-1,4-dialkoxybenzenes with CAN. The overall hydrophilicity of the substrates does not appear to be a significant factor in determining the diquinone yield for these reactions.
Effects of reaction conditions on quinone/diquinone product ratios in the oxidation of 1,4-dimethoxybenzene derivatives with ceric ammonium nitrate
Love, Brian E.,Duffy, Brian C.,Simmons, Alexander L.
supporting information, p. 1994 - 1997 (2014/04/03)
Proper choice of reaction conditions allows formation of either the quinone or corresponding diquinone as the major product upon treatment of 2-alkyl-1,4-dimethoxybenzenes with ceric ammonium nitrate.
Improved synthesis of diquinones
Love, Brian E.,Bonner-Stewart, Jeffrey,Forrest, Lori A.
body text, p. 813 - 817 (2009/06/19)
Preparation of a series of substituted diquinones is reported. In most examples, inverse order of addition (addition of a dimethoxybenzene derivative to a CAN solution) has been found to produce higher yields of diquinones than the traditional protocol in which the oxidant is added to the arene. Georg Thieme Verlag Stuttgart.
