44925-09-9 Usage
Uses
Used in Organic Synthesis:
2,2,2-Trichloroethyl acrylate is used as a reagent in organic synthesis for its high reactivity, enabling the creation of various chemical compounds and intermediates that are essential in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Polymerization Reactions:
As an acrylate ester, 2,2,2-Trichloroethyl acrylate is utilized in polymerization processes to produce polymers with specific properties. These polymers find applications in coatings, adhesives, and sealants due to their unique characteristics, such as durability, flexibility, and resistance to environmental factors.
Used in Chemical Research:
In the field of chemical research, 2,2,2-Trichloroethyl acrylate serves as a valuable compound for studying reaction mechanisms and exploring new synthetic pathways. Its reactivity allows researchers to investigate its behavior under various conditions, contributing to the advancement of chemical knowledge and innovation.
Used in Specialty Chemical Production:
2,2,2-Trichloroethyl acrylate is employed in the production of specialty chemicals that have specific applications in various industries. Its versatility in organic synthesis and polymerization reactions makes it a valuable component in the development of high-performance materials with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 44925-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,4,9,2 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 44925-09:
(7*4)+(6*4)+(5*9)+(4*2)+(3*5)+(2*0)+(1*9)=129
129 % 10 = 9
So 44925-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H5Cl3O2/c1-2-4(9)10-3-5(6,7)8/h2H,1,3H2
44925-09-9Relevant articles and documents
The 'Baylis - Hillman reaction' mechanism and applications revisited
Fort, Yves,Berthe, Marie Christine,Caubere, Paul
, p. 6371 - 6384 (2007/10/02)
It is shown that reaction of aryl, benzyl, alkyl and functionalised alkyl acrylic esters with benzaldehyde, in the presence of 1,4-diazabicyclo[2.2.2] octane, strongly depends upon the electronic and steric effects of the ester part. This influence is also observed in condensation of furfuraldehyde. Moreover, for the first time, it is shown that the overall condensation is equilibrated.
