13224-48-1 Usage
Molecular structure
1,2-di(biphenyl-4-yl)-1,2-diphenylethane-1,2-diol has a complex molecular structure consisting of two biphenyl groups and two phenyl groups attached to a central ethane-1,2-diol molecule.
Aromatic rings
The compound contains multiple aromatic rings, specifically two biphenyl and two phenyl groups, which contribute to its unique properties.
Hydroxyl groups
The presence of two hydroxyl (-OH) groups in the central ethane-1,2-diol molecule allows for potential hydrogen bonding and interactions with other molecules.
Industrial applications
Due to its unique structure and properties, 1,2-di(biphenyl-4-yl)-1,2-diphenylethane-1,2-diol may have potential applications in various industries, such as the development of new materials, pharmaceuticals, or advanced electronic devices.
Research potential
Further study and exploration of this compound's properties and potential applications are warranted to fully understand its significance and potential utility.
Physical properties
The compound's physical properties, such as melting point, boiling point, and solubility, are likely influenced by its complex molecular structure and the presence of aromatic rings and hydroxyl groups.
Chemical properties
The compound's chemical properties, including reactivity, stability, and potential for chemical modifications, are also influenced by its molecular structure and functional groups.
Molecular weight
The molecular weight of 1,2-di(biphenyl-4-yl)-1,2-diphenylethane-1,2-diol is determined by the sum of the atomic weights of all the atoms in its molecular structure.
Polarity
The presence of hydroxyl groups and aromatic rings in the molecule may result in a polar character, which can affect its solubility and interactions with other polar or nonpolar molecules.
Crystal structure
The arrangement of molecules in a crystalline form, if applicable, can provide insights into the compound's stability, mechanical properties, and potential applications in materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 13224-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,2 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13224-48:
(7*1)+(6*3)+(5*2)+(4*2)+(3*4)+(2*4)+(1*8)=71
71 % 10 = 1
So 13224-48-1 is a valid CAS Registry Number.
13224-48-1Relevant articles and documents
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Hatt,Pilgrim,Stephenson
, p. 478,480 (1941)
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Oxidative carbon-carbon bond cleavage of 1,2-diols to carboxylic acids/ketones by an inorganic-ligand supported iron catalyst
Chen, Weiming,Xie, Xin,Zhang, Jian,Qu, Jian,Luo, Can,Lai, Yaozhu,Jiang, Feng,Yu, Han,Wei, Yongge
supporting information, p. 9140 - 9146 (2021/11/23)
The carbon-carbon bond cleavage of 1,2-diols is an important chemical transformation. Although traditional stoichiometric and catalytic oxidation methods have been widely used for this transformation, an efficient and valuable method should be further explored from the views of reusable catalysts, less waste, and convenient procedures. Herein an inorganic-ligand supported iron catalyst (NH4)3[FeMo6O18(OH)6]·7H2O was described as a heterogeneous molecular catalyst in acetic acid for this transformation in which hydrogen peroxide was used as the terminal oxidant. Under the optimized reaction conditions, carbon-carbon bond cleavage of 1,2-diols could be achieved in almost all cases and carboxylic acids or ketones could be afforded with a high conversion rate and high selectivity. Furthermore, the catalytic system was used efficiently to degrade renewable biomass oleic acid. Mechanistic insights based on the observation of the possible intermediates and control experiments are presented.
InCl3/Al mediated pinacol coupling reactions of aldehydes and?ketones in aqueous media
Wang, Chunyan,Pan, Yuanjiang,Wu, Anxin
, p. 429 - 434 (2007/10/03)
A systematic work on the homo-pinacol coupling reactions of benzophenones, aldehydes, and acetophenones in aqueous media with InCl3/Al is described for the first time, in which various 1,2-diols are obtained in moderate to good yields.
