3183-43-5 Usage
Uses
Used in Pharmaceutical Industry:
2,2-Dimethyl-3-oxocyclobutanecarboxylic acid is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique structure allows it to be a key component in the development of new drugs, potentially offering novel therapeutic applications.
Used in Chemical Research:
2,2-Dimethyl-3-oxocyclobutanecarboxylic acid is used as a research compound in the field of organic chemistry. Its properties and reactivity can be studied to gain insights into the behavior of cyclobutanecarboxylic acid derivatives, which may lead to the discovery of new chemical reactions and applications.
Used in Material Science:
2,2-Dimethyl-3-oxocyclobutanecarboxylic acid is used as a building block in the development of new materials with specific properties. Its incorporation into polymers or other materials may result in unique characteristics, such as improved strength, flexibility, or chemical resistance, depending on the application.
Check Digit Verification of cas no
The CAS Registry Mumber 3183-43-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3183-43:
(6*3)+(5*1)+(4*8)+(3*3)+(2*4)+(1*3)=75
75 % 10 = 5
So 3183-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O3/c1-7(2)4(6(9)10)3-5(7)8/h4H,3H2,1-2H3,(H,9,10)
3183-43-5Relevant academic research and scientific papers
SUBSTITUTED DIAMINOPYRIMIDYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH
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Paragraph 0207; 0257, (2015/07/02)
Provided herein are diaminopyrimidyl Compounds having the following structures: wherein X, L, R1, and R2 are as defined herein, compositions comprising an effective amount of a Diaminopyrimidyl Compound, and methods for treating or preventing PKC-theta-mediated disorders, or a condition treatable or preventable by inhibition of a kinase, for example, PKC-theta.
A Practical synthesis of 3-Acyl cyclobutanones by [2 〈 2] annulation. Mechanism and utility of the zn(II)-Catalyzed condensation of r-Chloroenamines with electron-deficient alkenes
O'Brien, Jeannette M.,Kingsbury, Jason S.
experimental part, p. 1662 - 1672 (2011/05/12)
New conditions for the conversion of simple tertiary amides to R-chloroenamines and their use in Zn(II)-catalyzed cycloaddition reactions with commercial α,β-unsaturated carbonyl compounds allows rapid, regiocontrolled access to 3-acyl cyclobutanones. Rea
