206756-25-4 Usage
Description
2-Chloromethoxy-1,1,3,3,3-pentafluoro-propene is an organic compound characterized by its unique molecular structure, featuring a chloromethoxy group and five fluorine atoms attached to a propene backbone. 2-Chloromethoxy-1,1,3,3,3-pentafluoro-propene is known for its reactivity and utility in various chemical reactions, particularly in the field of synthetic chemistry.
Uses
Used in Synthetic Chemistry:
2-Chloromethoxy-1,1,3,3,3-pentafluoro-propene is used as a reagent for halogen-exchange reactions, which are crucial in the synthesis of various organic compounds. Its presence as a fluoride source allows for the selective replacement of other halogens in a molecule, facilitating the formation of new chemical entities with different properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Chloromethoxy-1,1,3,3,3-pentafluoro-propene can be utilized as a building block for the development of novel drugs. Its unique structure and reactivity make it a valuable component in the synthesis of complex molecular architectures, potentially leading to the discovery of new therapeutic agents.
Used in Material Science:
The compound can also be employed in the field of material science, where its fluorine-rich structure may contribute to the development of new materials with enhanced properties, such as improved chemical stability, thermal resistance, or non-stick surfaces.
Check Digit Verification of cas no
The CAS Registry Mumber 206756-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,7,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 206756-25:
(8*2)+(7*0)+(6*6)+(5*7)+(4*5)+(3*6)+(2*2)+(1*5)=134
134 % 10 = 4
So 206756-25-4 is a valid CAS Registry Number.
206756-25-4Relevant articles and documents
METHODS FOR PREPARING FLUORINATED VINYL ETHERS
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Page/Page column 5, (2010/11/03)
A method for preparing a fluorinated vinyl ether compound comprising reacting a fluorinated ether substrate having (i) a hydrogen atom on a carbon atom that is alpha to an etheric oxygen and (ii) a fluorine atom on a carbon atom that is beta to the etheric oxygen, with an organolithium base to provide a reaction product comprising a fluorinated vinyl ether compound.
