82832-29-9 Usage
Uses
Since the provided materials do not specify the exact uses of Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]-, it is not possible to list its applications based on the given information. However, given its unique structure, it is likely that Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]- could be used in various applications such as:
Used in Chemical Industry:
Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]could be used as an intermediate in the synthesis of other complex organic compounds or as a building block for the development of new materials with specific properties.
Used in Pharmaceutical Industry:
Due to its unique molecular structure, Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]- may have potential applications in the pharmaceutical industry as a precursor for the development of new drugs or as a modifier to enhance the properties of existing pharmaceutical compounds.
Used in Material Science:
Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]-'s fluorinated nature and the presence of a bicyclohexyl moiety may make it suitable for use in the development of new materials with specific properties, such as improved thermal stability, chemical resistance, or other desirable characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 82832-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,3 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82832-29:
(7*8)+(6*2)+(5*8)+(4*3)+(3*2)+(2*2)+(1*9)=139
139 % 10 = 9
So 82832-29-9 is a valid CAS Registry Number.
82832-29-9Relevant academic research and scientific papers
Iron-catalysed fluoroaromatic coupling reactions under catalytic modulation with 1,2-bis(diphenylphosphino)benzene
Hatakeyama, Takuji,Kondo, Yoshiyuki,Fujiwara, Yu-Ichi,Takaya, Hikaru,Ito, Shingo,Nakamura, Eiichi,Nakamura, Masaharu
supporting information; experimental part, p. 1216 - 1218 (2009/07/10)
A catalytic amount of 1,2-bis(diphenylphosphino)benzene (DPPBz) achieves selective cleavage of sp3-carbon-halogen bond in the iron-catalysed cross-coupling between polyfluorinated arylzinc reagents and alkyl halides, which was unachievable with
Iron-catalyzed cross-coupling of alkyl sulfonates with arylzinc reagents
Ito, Shingo,Fujiwara, Yu-Ichi,Nakamura, Eiichi,Nakamura, Masaharu
supporting information; experimental part, p. 4306 - 4309 (2009/12/26)
Iron-catalyzed cross-coupling reactions of primary and secondary alkyl sulfonates with arylzinc reagents proceed smoothly In the presence of excess TMEDA and a concomitant magnesium salt. The arylzinc reagents are prepared from the corresponding aryllithium or magnesium reagents with ZnI2. The In situ formation of alkyl Iodides and consecutive rapid cross-coupling avoids discrete preparation of the unstable secondary alkyl halides and also achieves high product selectivity.
Reduction of 3-Substituted 1-Arylcyclobutanols
Kinnius, Joerg,Dehmlow, Eckehard Volker
, p. 421 - 423 (2007/10/03)
A useful and specific method for the the title reaction (1 → 2) involves treatment with NaBH4 in CF3COOH whereas other procedures from the literature yield hard-to-separate mixtures. 1-Arylcyclohexanols 3 give mainly cyclohexenes with borohydride/trifluoroacetic acid. Their reduction to compounds 4 ,however, is possible with MeSO3H/ NaBH4.
