110482-96-7 Usage
Description
Ethyl 2,2-difluoropent-4-enoate, also known as ethyl 2,2-difluoro-4-pentenoate, is a chemical compound with the molecular formula C6H8F2O2. It is an ester, which is a type of organic compound formed by the reaction of an alcohol and an organic acid. This particular ester is characterized by the presence of two fluorine atoms, which are attached to the carbon atoms in the molecule. Its unique chemical structure, low boiling point, and strong odor make it a versatile compound in various applications.
Uses
Used in Organic Synthesis:
Ethyl 2,2-difluoropent-4-enoate is used as a building block in organic synthesis for the production of other chemical compounds. Its unique structure allows for the creation of a wide range of molecules with diverse properties and applications.
Used as a Solvent:
Due to its low boiling point and strong odor, Ethyl 2,2-difluoropent-4-enoate is used as a solvent in some applications. Its ability to dissolve certain substances makes it a valuable component in various chemical processes.
Used in Pharmaceutical Development:
Ethyl 2,2-difluoropent-4-enoate may have potential applications in the development of pharmaceuticals due to its unique chemical structure. Its properties can be harnessed to create new drugs with specific therapeutic effects.
Used in Agrochemical Development:
Similarly, Ethyl 2,2-difluoropent-4-enoate may also be utilized in the development of agrochemicals. Its unique structure can contribute to the creation of new compounds with potential applications in agriculture, such as pesticides or herbicides.
Check Digit Verification of cas no
The CAS Registry Mumber 110482-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,4,8 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110482-96:
(8*1)+(7*1)+(6*0)+(5*4)+(4*8)+(3*2)+(2*9)+(1*6)=97
97 % 10 = 7
So 110482-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H10F2O2/c1-3-5-7(8,9)6(10)11-4-2/h3H,1,4-5H2,2H3
110482-96-7Relevant articles and documents
Radical reaction using an organocopper reagent derived from ethyl bromodifluoroacetate
Sato, Kazuyuki,Ogawa, Yuko,Tamura, Misato,Harada, Mika,Ohara, Terumasa,Omote, Masaaki,Ando, Akira,Kumadaki, Itsumaro
, p. 1285 - 1295 (2002)
In our previous work, reaction of ethyl bromodifluoroacetate (1) in the presence of Cu powder with olefins activated by an electron-withdrawing group gave the Michael-type adducts through an anionic intermediate. The same reaction with non-activated olefi
Preparative Flow Techniques; 1. Low-Temperature Organometallic Reactions: Synthesis of Ethyl 2,2-Difluoro-4-pentenoate
Kolb, Michael,Gerhart, Fritz,Francois, Jean-Paul
, p. 469 - 470 (1988)
A convenient preparation of the synthetically useful ethyl 2,2-difluoro-4-pentenoate using the low-temperature flow technique is described.The method is suitable for small-scale as well as for large-scale application.
Synthesis and biological evaluation of new bicyclic fluorinated uracils through ring-closing metathesis
Fustero, Santos,Catalan, Silvia,Piera, Julio,Sanz-Cervera, Juan F.,Fernandez, Begona,Acena, Jose Luis
, p. 4010 - 4013 (2007/10/03)
Two families of bicyclic fluorinated uracils have been prepared starting from a gem-difluorinated unsaturated nitrile, by means of a ring-closing metathesis reaction to form the new ring, which is fused at the C-5/C-6 or N-1/C-6 positions of the uracil mo
