62012-58-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
A derivative is a compound that is structurally related to another compound, in this case, biphenyl.
Explanation
Biphenyl derivatives are a class of organic compounds that have a biphenyl backbone with additional functional groups attached.
Explanation
Biphenyl and its derivatives are used in various industries, including the production of dyes, explosives, and pesticides.
Explanation
The specific arrangement of atoms and functional groups in the molecule, which gives it its unique properties.
Explanation
The compound may help prevent the degradation of materials by heat or oxygen, making it useful as a stabilizer or antioxidant.
Explanation
The compound may serve as a building block or intermediate in the synthesis of other chemical compounds.
Explanation
As with any chemical, it is important to follow safety guidelines and precautions to minimize risks associated with handling and use.
Derivative of biphenyl
Yes
Type of organic compound
Biphenyl derivative
Common uses
Dyes, explosives, and pesticides
Chemical structure
Six methyl groups and two phenylmethoxy groups attached to the biphenyl backbone
Potential applications
Stabilizer or antioxidant in materials such as plastics and rubbers
Utility in organic synthesis
Yes
Safety precautions
Proper handling and safety measures should be taken
Check Digit Verification of cas no
The CAS Registry Mumber 62012-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,1 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62012-58:
(7*6)+(6*2)+(5*0)+(4*1)+(3*2)+(2*5)+(1*8)=82
82 % 10 = 2
So 62012-58-2 is a valid CAS Registry Number.
62012-58-2Relevant articles and documents
Thallium in Organic Synthesis. 58. Regiospecific Intermolecular Oxidative Dehydrodimerization of Aromatic Compounds to Biaryls Using Thallium (III) Trifluoroacetate
McKillop, Alexander,Turrell, Andrew G.,Young, Derek W.,Taylor, Edward C.
, p. 6504 - 6512 (1980)
Treatment of a variety of aromatic substrates with thallium(III) trifluoroacetate (TTFA) in trifluoroacetic acid (TFA), or in carbon tetrachloride or acetonitrile containing boron trifluoride etherate, results in smooth, rapid, and direct regiospecific oxidative dehydrodimerization to give symmetrical biaryls in good to excellent yield.The method is particularly useful when applied to substrates in which the ring substituents are either electron donating or mildly electron withdrawing.Aromatic substrates which contain powerful electron-withdrawing groups (CN, COOR, NO2) fail to react.The reaction is postulated to proceed via (a) reaction of TTFA with the aromatic substrate and generation of the radical cation Ar+; (b) reaction of this electrophile with the aromatic substrate; (c) oxidative aromatization of the intermediate thus produced by TTFA.Biaryls can be obtained similarly by oxidation of the same substrates with either mercury(II) trifluoroacetate in TFA containing boron trifluoride, lead(IV) acetate in acetonitrile containing boron trifluoride, iron(III) chloride in methylene chloride, or cobalt(III) fluoride in TFA.Yields in the Hg(II) and Fe(III) reactions are generally inferior to those obtained with TTFA, but those obtained in the Pb(IV) and Co(III) oxidations are in many instances comparable to, or even better than, the TTFA results.The oxidations with Hg(II), Pb(IV), Fe(III), and CO(III) are also postulated to proceed via a radical cation mechanism.
