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1,2-Cyclohexanediol, 4-tert-butyl-1-phenyl, stereoisomer is a complex organic compound with a molecular formula of C14H22O2. It is a stereoisomer, meaning it has the same molecular formula as other compounds within the same family but differs in the spatial arrangement of its atoms. This specific compound features a cyclohexane ring with two hydroxyl groups at the 1 and 2 positions, a tert-butyl group at the 4 position, and a phenyl group at the 1 position. Due to the presence of stereocenters, 1,2-Cyclohexanediol, 4-tert-butyl-1-phenyl-, stereoisomer can exist in various stereoisomeric forms, which can significantly impact its physical and chemical properties. It is important to note that the specific stereochemistry of the compound is not provided in the name, and further information would be required to determine the exact spatial arrangement of the atoms.

4127-41-7

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4127-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4127-41-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,2 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4127-41:
(6*4)+(5*1)+(4*2)+(3*7)+(2*4)+(1*1)=67
67 % 10 = 7
So 4127-41-7 is a valid CAS Registry Number.

4127-41-7Downstream Products

4127-41-7Relevant academic research and scientific papers

An investigative study of kinetic resolutions by the Sharpless asymmetric dihydroxylation reaction

Hamon, David P.G,Tuck, Kellie L,Christie, Hamish S

, p. 9499 - 9508 (2007/10/03)

The requirements for a highly selective kinetic resolution with the Sharpless asymmetric dihydroxylation (AD) reaction were investigated with a number of alkene substrates. It was found that with 1-phenyl-4-tert-butylcyclohexene enantioselectivity is very high, yet diastereoselectivity is poor and kinetic resolution is ineffective. With 5-methyl-2-phenylbicyclo[3.2.0]heptan-2-ene both diastereoselectivity and enantioselectivity are high and kinetic resolution is effective. It was discovered that the transition state for the product-determining step in the Sharpless AD reaction is not product-like, and effective kinetic resolution can occur when one face of a chiral alkene is hindered.

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