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(-)-(R)-2-Benzylidene-5-methylcyclohexanone is a chiral organic compound characterized by its unique molecular structure. It features a cyclohexanone ring with a methyl group at the 5-position and a benzylidene group at the 2-position. The compound exhibits optical activity due to its chiral center, with the R configuration at the 2-position. This molecule is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of stereochemistry. Its specific properties, such as solubility and reactivity, can be influenced by the presence of the benzylidene and methyl groups, making it a valuable compound for various chemical and pharmaceutical applications.

7577-00-6

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7577-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7577-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7577-00:
(6*7)+(5*5)+(4*7)+(3*7)+(2*0)+(1*0)=116
116 % 10 = 6
So 7577-00-6 is a valid CAS Registry Number.

7577-00-6Downstream Products

7577-00-6Relevant academic research and scientific papers

Asymmetric Induction in Diels-Alder Reactions to Acrylates Derived from Chiral sec-Alcohols

Oppolzer, Wolfgang,Kurth, Mark,Reichlin, Daniel,Chapuis, Christian,Mohnhaupt, Martin,Moffatt, Frank

, p. 2802 - 2807 (1981)

Starting from the enantiomerically pure monoterpenes (+)-pulegone (3), (+)-limonene (7), (-)-β-pinene (9), (+)- and (-)-camphor (13) or (+)-cholestenone (11) the chiral alcohols 4, 5, 6, 8, 10, 12, 14, 15, 16, 17 and 18 were prepared; their acrylates II underwent a TiCl4-promoted Diels-Alder addition to cyclopentadiene (Scheme 3, Table) giving in a predictable manner either the (2R)- or the (2S)-adducts III with 63 to 88percent asymmetric induction.

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