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1-Hydroxy-α-methyl-α-phenyl-cyclopentanemethanol, also known as 1-hydroxy-α-methyl-α-phenyl-cyclopentane-1-methanol, is a complex organic compound with the molecular formula C13H18O2. It is a cycloalkane derivative, featuring a cyclopentane ring with a hydroxyl group (-OH), a methyl group (-CH3), and a phenyl group (C6H5) attached to the α-carbon. 1-hydroxy-α-methyl-α-phenyl-cyclopentanemethanol is characterized by its unique structure, which combines the properties of a cycloalkane with those of a phenol and an alcohol. It is synthesized through various chemical reactions and can be used in the pharmaceutical and chemical industries for the development of drugs, fragrances, and other specialty chemicals. Due to its specific functional groups and structural features, 1-hydroxy-α-methyl-α-phenyl-cyclopentanemethanol has potential applications in the synthesis of more complex molecules and as an intermediate in organic synthesis.

4235-11-4

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4235-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4235-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4235-11:
(6*4)+(5*2)+(4*3)+(3*5)+(2*1)+(1*1)=64
64 % 10 = 4
So 4235-11-4 is a valid CAS Registry Number.

4235-11-4Relevant academic research and scientific papers

Electroreductive crossed pinacol coupling of aromatic ketones with aliphatic ketones and aldehydes

Kise, Naoki,Shiozawa, Yousuke,Ueda, Nasuo

, p. 5415 - 5426 (2007)

The intermolecular crossed pinacol coupling of aromatic ketones with aliphatic aldehydes and ketones was effected by electroreduction in the presence of chlorotrimethylsilane. The best result was obtained using a Pb cathode in Bu4NPF6/sub

Mg-promoted mixed pinacol coupling

Maekawa, Hirofumi,Yamamoto, Yoshimasa,Shimada, Hisashi,Yonemura, Kazuaki,Nishiguchi, Ikuzo

, p. 3869 - 3872 (2007/10/03)

Mg-promoted reduction of a mixture of aromatic ketones (or imines) and aliphatic carbonyl compounds in N,N-dimethylformamide (DMF) brought about unique mixed pinacol type of cross coupling to give unsymmetrical vicinal diols (or amino alcohols) or α-hydroxyketones in good to moderate yields. The reaction may be initiated by electron transfer from magnesium metal to an aromatic carbonyl compound possessing a less negative reduction potential. The difference of reduction potential between aromatic ketones (or imines) and aliphatic carbonyl compounds was found to be one of the important key factors in this selective cross coupling.

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