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1-Ref-Acetyl-4-trans-tert.-butyl-cyclohexanol-(1-trans) is a complex organic chemical compound with the molecular formula C13H22O2. It is a derivative of cyclohexanol, featuring a cyclohexane ring with a trans-tert-butyl group at the 4-position and an acetyl group at the 1-position. 1-ref-Acetyl-4-trans-tert.-butyl-cyclohexanol-(1-trans) is characterized by its unique stereochemistry, with the trans configuration indicating that the substituents on the cyclohexane ring are on opposite sides of the ring. It is synthesized through a series of chemical reactions and is used in various applications, such as in the pharmaceutical industry for the synthesis of drugs and in the fragrance industry for creating unique scents. The compound's specific properties, such as its melting point, boiling point, and solubility, are crucial for its practical applications and handling.

6555-57-3

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6555-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6555-57-3 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 6555-57:
(6*6)+(5*5)+(4*5)+(3*5)+(2*5)+(1*7)=113
113 % 10 = 3
So 6555-57-3 is a valid CAS Registry Number.

6555-57-3Relevant 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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