29263-83-0 Usage
Uses
Used in Pharmaceutical Industry:
DIETHYL ETHYLCHLOROMALONATE is used as a key intermediate for the production of pharmaceuticals due to its ability to participate in esterification and condensation reactions, facilitating the synthesis of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, DIETHYL ETHYLCHLOROMALONATE is utilized as a reagent in the synthesis of agrochemicals, contributing to the development of pesticides and other agricultural products.
Used in Organic Synthesis:
DIETHYL ETHYLCHLOROMALONATE is used as a building block in organic synthesis for creating complex organic molecules, highlighting its versatility and importance in the field of chemistry.
Used in Medicinal Chemistry:
DIETHYL ETHYLCHLOROMALONATE is employed as a valuable component in medicinal chemistry, where it aids in the development and synthesis of potential drug candidates, underlining its significance in advancing pharmaceutical research.
Safety Note:
DIETHYL ETHYLCHLOROMALONATE is a potential irritant, and it is crucial to handle it with care in a laboratory setting to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 29263-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,6 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29263-83:
(7*2)+(6*9)+(5*2)+(4*6)+(3*3)+(2*8)+(1*3)=130
130 % 10 = 0
So 29263-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H15ClO4/c1-4-9(10,7(11)13-5-2)8(12)14-6-3/h4-6H2,1-3H3
29263-83-0Relevant academic research and scientific papers
Phase transfer catalyzed halogenation of carbon acids
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, (2008/06/13)
A process is disclosed for chlorinating, brominating and/or iodinating an organic substrate containing both a single acidic hydrogen atom and at least one electron withdrawing group attached to the same carbon atom. The process replaces the single acidic hydrogen with chlorine, bromine and/or iodine and involves reacting the substrate in solution with a halogenating agent (e.g., a perhalomethane wherein the halogen substituents are I, Br and/or Cl, a trihaloacetic acid ester wherein the halogen substituents are Br and/or Cl, or a perfluoroalkyl halide wherein the halide is I, Br and/or Cl) in the presence of (i) a phase transfer catalyst of the formula R1 R2 R3 R4 LJ where L is selected from the group consisting of phosphorus and nitrogen, where J is an inorganic anion other than fluoride, and where R1, R2, R3 and R4 are independently chosen from the froup consisting of hydrocarbyl radicals containing from 1 to about 20 carbon atoms and (ii) a mild inorganic base which is insoluble in the reaction medium.
