68525-41-7 Usage
Molecular structure
The compound consists of a benzene ring with two chlorine atoms attached, and a substituted butyl group with a tert-butyl moiety and a 4-chlorophenyl group.
Optical activity
The compound is optically active, meaning it can rotate plane-polarized light.
Chiral center
The compound has a chiral center at the tert-butyl carbon, which gives it stereoisomers.
Stereoisomers
The compound exists in two enantiomeric forms, (1R,2S) and (1S,2R), which are non-superimposable mirror images of each other.
Synthetic compound
It is a synthetic compound, meaning it is not found naturally and is created through chemical synthesis.
Pharmaceutical and research applications
The compound is used in pharmaceutical and research applications, although the specific uses depend on the context and purpose.
Solubility
The solubility of the compound is not specified in the provided material, but it is likely to be soluble in organic solvents due to its nonpolar nature.
Stability
The stability of the compound is not specified in the provided material, but it is likely to be stable under normal conditions due to the presence of the aromatic benzene ring.
Reactivity
The reactivity of the compound is not specified in the provided material, but it may be susceptible to reactions involving the chlorine atoms or the tert-butyl moiety.
Toxicity
The toxicity of the compound is not specified in the provided material, but it should be handled with care due to its complex and potentially reactive structure.
Check Digit Verification of cas no
The CAS Registry Mumber 68525-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,2 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68525-41:
(7*6)+(6*8)+(5*5)+(4*2)+(3*5)+(2*4)+(1*1)=147
147 % 10 = 7
So 68525-41-7 is a valid CAS Registry Number.
68525-41-7Relevant articles and documents
Thermolabile Hydrocarbons, XVIII. 1-Substituted Neopentyl radicals and their Dimers
Eichin, Karl-Heinz,Beckhaus, Hans-Dieter,Hellmann, Siegried,Fritz, Hans,Peters, Eva-Maria,et al.
, p. 1787 - 1821 (2007/10/02)
Five 3,4-diaryl-2,2,5,5-tetramethylhexanes 1a - e were prepared as pure meso- and DL-isomers.According to the NMR spectra, x-ray analyses for meso- and DL-1e (with an (FB)2E conformation as energy minimum for DL-1e), and force field calculations the diastereomers have distinctly different minimum energy conformations, rotational potentials, and strain enthalpies.Also the activation parameters for the thermal dissociation into 1-arylneopentyl radicals 2 are typically differing.From an entropy discussion it is concluded that sandwich-like diastereomeric radical complexes are formed in these reactions as first intermediates.Their tightness influences ΔS%.The recombinations of the radicals 2 likewise take place stereoselectively.Their substituent effects on the selectivity can also be understood by primary formation of diastereomeric complexes of radical pairs.
