134176-20-8 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
(1alpha,6alpha,7alpha)-2-Oxobicyclo[4.1.0]heptane-7-carboxylic acid methyl ester is used as a key intermediate in the synthesis of pharmaceutical compounds due to its potential medicinal properties and biological activities. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Organic Synthesis:
In the field of organic synthesis, (1alpha,6alpha,7alpha)-2-Oxobicyclo[4.1.0]heptane-7-carboxylic acid methyl ester serves as a versatile building block for the preparation of complex organic molecules. Its ketone and carboxylic acid functional groups enable various chemical reactions, facilitating the synthesis of a wide range of compounds.
Used in Materials Science:
(1alpha,6alpha,7alpha)-2-Oxobicyclo[4.1.0]heptane-7-carboxylic acid methyl ester is utilized in materials science for the development of novel materials with specific properties. Its unique structure and functional groups can be exploited to create materials with tailored characteristics for various applications.
Used in Chemical Engineering:
In chemical engineering, (1alpha,6alpha,7alpha)-2-Oxobicyclo[4.1.0]heptane-7-carboxylic acid methyl ester is employed in the design and optimization of chemical processes. Its unique properties and reactivity can be harnessed to improve process efficiency, yield, and selectivity in the production of various chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 134176-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,7 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 134176-20:
(8*1)+(7*3)+(6*4)+(5*1)+(4*7)+(3*6)+(2*2)+(1*0)=108
108 % 10 = 8
So 134176-20-8 is a valid CAS Registry Number.
134176-20-8Relevant academic research and scientific papers
Platinum-Catalyzed α,β-Desaturation of Cyclic Ketones through Direct Metal–Enolate Formation
Chen, Ming,Dong, Guangbin
supporting information, p. 7956 - 7961 (2021/03/01)
The development of a platinum-catalyzed desaturation of cyclic ketones to their conjugated α,β-unsaturated counterparts is reported in this full article. A unique diene-platinum complex was identified to be an efficient catalyst, which enables direct metal-enolate formation. The reaction operates under mild conditions without using strong bases or acids. Good to excellent yields can be achieved for diverse and complex scaffolds. A wide range of functional groups, including those sensitive to acids, bases/nucleophiles, or palladium species, are tolerated, which represents a distinct feature from other known desaturation methods. Mechanistically, this platinum catalysis exhibits a fast and reversible α-deprotonation followed by a rate-determining β-hydrogen elimination process, which is different from the prior Pd-catalyzed desaturation method. Promising preliminary enantioselective desaturation using a chiral-diene-platinum complex has also been obtained.
