306935-33-1 Usage
General Description
Methyl 2-chloro-4,4-dimethyl-3-oxopentanoate is a chemical compound with the molecular formula C8H13ClO3. It is a colorless to pale yellow liquid that is used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. METHYL 2-CHLORO-4,4-DIMETHYL-3-OXOPENTANOATE is classified as an ester, containing a chlorine atom and two methyl groups on the carbon chain. It is commonly utilized in organic synthesis reactions, particularly in the production of various drugs and pesticides. The compound's structure and properties make it a versatile building block for creating complex organic molecules. However, it is important to handle this chemical with care, as it is a potentially hazardous substance that should be used in accordance with proper safety procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 306935-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,3 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 306935-33:
(8*3)+(7*0)+(6*6)+(5*9)+(4*3)+(3*5)+(2*3)+(1*3)=141
141 % 10 = 1
So 306935-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H13ClO3/c1-8(2,3)6(10)5(9)7(11)12-4/h5H,1-4H3
306935-33-1Relevant articles and documents
Design, synthesis, and biological evaluation of thiazoles targeting flavivirus envelope proteins
Mayhoub, Abdelrahman S.,Khaliq, Mansoora,Kuhn, Richard J.,Cushman, Mark
scheme or table, p. 1704 - 1714 (2011/05/05)
A series of third-generation analogues of methyl 4-(dibromomethyl)-2-(4- chlorophenyl)thiazole-5-carboxylate (1), which had the most potent antiviral activity among the first- and second-generation compounds, have been synthesized and tested against yellow fever virus using a cell-based assay. The compounds were designed with the objectives of improving metabolic stability, therapeutic index, and antiviral potency. The biological effects of C4 and C5 substitution were examined. The methylthio ester and the dihydroxypropylamide analogues had the best antiviral potencies and improved therapeutic indices and metabolic stabilities relative to the parent compound 1.
