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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 consists of a heptane backbone with three methyl groups at positions 2, 3, and 6, and a phenyl group attached to the first carbon. The compound features a 1,5-dione functional group, which means it has two carbonyl groups separated by three carbon atoms. The stereochemistry at positions 2 and 3 is R, indicating that the hydrogen atoms and the phenyl group are on the same side of the molecule when viewed from the perspective of the double bond. (2R,3R)-2,3,6-Trimethyl-1-phenyl-heptane-1,5-dione is an example of a complex organic molecule with potential applications in various fields, such as pharmaceuticals or chemical research, due to its specific structural features and chirality.

95741-07-4

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95741-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95741-07-4 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 95741-07:
(7*9)+(6*5)+(5*7)+(4*4)+(3*1)+(2*0)+(1*7)=154
154 % 10 = 4
So 95741-07-4 is a valid CAS Registry Number.

95741-07-4Downstream Products

95741-07-4Relevant 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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