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(2R,3R)-2,3,6-Trimethyl-1-phenyl-heptane-1,5-dione is a chiral organic compound characterized by its unique molecular structure. It features a heptane backbone with three methyl groups at positions 2, 3, and 6, and a phenyl group attached to the first carbon. The molecule also contains two carbonyl groups at positions 1 and 5, which are crucial for its reactivity and properties. (2R,3R)-2,3,6-Trimethyl-1-phenyl-heptane-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 organic chemistry and may have applications in the synthesis of pharmaceuticals and other specialty chemicals due to its structural complexity and potential for functional group manipulation.

95741-08-5

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95741-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95741-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,4 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95741-08:
(7*9)+(6*5)+(5*7)+(4*4)+(3*1)+(2*0)+(1*8)=155
155 % 10 = 5
So 95741-08-5 is a valid CAS Registry Number.

95741-08-5Downstream Products

95741-08-5Relevant 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 (1986)

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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