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1β-Acetyl-4β-t-butyl-1α-cyclohexanol is a complex organic compound with the molecular formula C12H22O2. It is a derivative of cyclohexanol, featuring an acetyl group (-COCH3) at the 1β position and a t-butyl group (-C(CH3)3) at the 4β position. 1β-Acetyl-4β-t-butyl-1α-cyclohexanol is characterized by its unique structure, which includes a six-carbon cyclohexane ring with two substituents at different positions. The acetyl group provides a ketone functionality, while the t-butyl group introduces a bulky, sterically hindered alkyl substituent. This combination of functional groups and steric hindrance can influence the compound's reactivity, solubility, and physical properties, making it potentially useful in various chemical applications, such as in the synthesis of pharmaceuticals or as a chiral auxiliary in asymmetric reactions.

6555-58-4

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6555-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6555-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6555-58:
(6*6)+(5*5)+(4*5)+(3*5)+(2*5)+(1*8)=114
114 % 10 = 4
So 6555-58-4 is a valid CAS Registry Number.

6555-58-4Relevant academic research and scientific papers

Electroorganic Chemistry. 140. Electroreductively Intra- and Intermolecular Couplings of Ketones with Nitriles

Shono, Tatsuya,Kise, Naoki,Fujimoto, Taku,Tominaga, Naoto,Morita, Hiroshi

, p. 7175 - 7187 (2007/10/02)

Electroreduction of γ- and δ-cyano ketones in i-PrOH with Sn cathode gave α-hydroxy ketones and their dehydroxylated ketones as the intramolecularly coupled products.Guaiazulene, (-)-valeranone, polyquinanes, dihydrojasmone, methyl dihydrojasmonate, and rosaprostol have been synthesized by utilizing this electroreductive intramolecular coupling of γ- and δ-cyano ketones in one of the key steps.Similarly, electroreduction of a mixture of ketone and nitrile gave the corresponding intermolecularly coupled product.The product obtained by the electroreductive intermolecular coupling of (+)-dihydrocarvone with acetonitrile has been found to be the precursor of an effective chiral ligand for the enantioselective addition of diethylzinc to aldehydes.

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