44925-09-9 Usage
General Description
2,2,2-Trichloroethyl acrylate is a chemical compound with the molecular formula C5H5Cl3O2. It is a colorless liquid with a pungent odor and is primarily used as a reagent in organic synthesis and polymerization reactions. Trichloroethyl acrylate is classified as an acrylate ester, which means it contains the acrylate functional group. 2,2,2-TRICHLOROETHYL ACRYLATE is a highly reactive and flammable substance that should be handled with caution in a controlled laboratory environment. It is also known to be a skin and eye irritant, as well as a potential respiratory hazard. Overall, 2,2,2-Trichloroethyl acrylate is a versatile chemical with various industrial applications, but it poses potential risks and should be handled and used with care.
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.
