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(2R,3R)-2,3-Dimethyl-1-phenyl-hexane-1,5-dione is a chiral organic compound characterized by its unique molecular structure. It features a hexane backbone with two methyl groups at the 2nd and 3rd carbon positions, and a phenyl group attached to the 1st carbon. The molecule also contains two carbonyl groups at the 1st and 5th positions, which are crucial for its reactivity and properties. (2R,3R)-2,3-Dimethyl-1-phenyl-hexane-1,5-dione is a specific enantiomer, with the R configuration at both the 2nd and 3rd carbons, which can influence its physical and chemical behavior differently from its mirror image enantiomer. It is important in the field of organic chemistry, particularly in the study of stereochemistry and the synthesis of chiral molecules, which are essential in pharmaceuticals and other industries.

25552-22-1

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25552-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25552-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,5 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25552-22:
(7*2)+(6*5)+(5*5)+(4*5)+(3*2)+(2*2)+(1*2)=101
101 % 10 = 1
So 25552-22-1 is a valid CAS Registry Number.

25552-22-1Downstream Products

25552-22-1Relevant academic research and scientific papers

INFLUENCE OF ENOLATE GEOMETRY ON THE STEREOCHEMISTRY OF MICHAEL ADDITIONS OF KETONE ENOLATES TO α, β-UNSATURATED KETONES

Oare, David A.,Heathcock, Clayton H.

, p. 6169 - 6172 (2007/10/02)

Preformed lithium enolates of ketones react with acyclic α,β-unsaturated ketones to give 1,5-diketones in good chemical yields.A strong correlation exists between enolate geometry and product stereochemistry; enolates having the Z configuration provide anti addition products while E enolates usually provide the syn diastereomers.

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