62173-55-1 Usage
Uses
Used in Organic Synthesis:
Dimethyl 2,3-dichlorosuccinate is used as a reagent in organic synthesis for the preparation of various derivatives. Its ability to undergo substitution reactions with nucleophiles allows for the creation of a variety of products, contributing to the development of new chemical entities.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Dimethyl 2,3-dichlorosuccinate is employed as a key intermediate in the synthesis of certain drugs. Its reactivity and the ease of forming new compounds make it a useful building block for medicinal chemistry, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
Dimethyl 2,3-dichlorosuccinate is utilized in chemical research to explore new reaction pathways and mechanisms. Its unique properties and reactivity provide opportunities for scientists to investigate and understand the behavior of succinate derivatives in various chemical contexts.
Safety Considerations:
Due to its potential health and environmental impacts, Dimethyl 2,3-dichlorosuccinate is considered a hazardous chemical. It should be handled with care, following appropriate safety protocols to minimize risks to both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 62173-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,7 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62173-55:
(7*6)+(6*2)+(5*1)+(4*7)+(3*3)+(2*5)+(1*5)=111
111 % 10 = 1
So 62173-55-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H8Cl2O4/c1-11-5(9)3(7)4(8)6(10)12-2/h3-4H,1-2H3
62173-55-1Relevant academic research and scientific papers
Forti, Luca
, p. 2509 - 2510 (1995)
Methyl 2-Br-2-Cl-carboxylates react with 1-octene in DMF/CH2Cl2 in a radical process promoted by CuBr/Fe, yielding 2-alkyl-2-Cl-4-Br-carboxylates smoothly and efficiently.
The formation of halogenated succinates by liquid-phase direct fluorination with elemental fluorine
Syvret, Robert G.,Vassilaros, Daniel L.,Parees, David M.,Pez, Guido P.
, p. 277 - 282 (2007/10/02)
Direct fluorination of maleic anhydride with elemental fluorine has been investigated in different solvents at low temperatures.It was discovered that the net conversion of maleic anhydride, as well as the overall yield and composition of the halogenated products, depend strongly on the experimental conditions employed.Fluorinations conducted in fluorotrichloromethane, chloroform or mixtures thereof, in the presence of sodium fluoride, resulted in good yields of halogenated succinic acid derivatives: the predominant products being 2,3-dihalogenated succinic acids.Product distributions varied widely between experiments conducted at 0 deg C and -25 deg C, and also between experiments conducted in neat CHCl3 and in CFCl3/CHCl3 mixtures.Experimental details and some comments regarding the stereoselectivity of halogen addition are provided.
