131469-67-5 Usage
Structure
2-[(4-CHLORO-PHENYL)-HYDROXY-METHYL]-ACRYLIC ACID METHYL ESTER The compound is formed by a hydroxymethyl group (-CH2OH) attached to a 4-chlorophenyl ring, which is connected to a methyl ester group (-OCH3) and a acrylic acid (-CH2-C=CH-COO-) moiety.
Methyl ester
The compound is a methyl ester of a hydroxymethyl acrylic acid derivative This means it has an ester functional group (-COO-) formed by the reaction of the hydroxymethyl group with the carboxylic acid group of acrylic acid, with an additional methyl group (-CH3) attached to the oxygen.
Industrial applications
It may be used as a base material for the production of polymers and resins This indicates that the compound can be further reacted and processed to create a variety of polymers and resins, which can be used in numerous applications such as coatings, adhesives, and plastics.
Health and environmental risks
It is important to handle this compound with care This suggests that improper handling or exposure to the compound may pose risks to human health and the environment. It is crucial to follow safety guidelines and regulations when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 131469-67-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,4,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131469-67:
(8*1)+(7*3)+(6*1)+(5*4)+(4*6)+(3*9)+(2*6)+(1*7)=125
125 % 10 = 5
So 131469-67-5 is a valid CAS Registry Number.
131469-67-5Relevant articles and documents
Studying the Morita-Baylis-Hillman Reaction in Continuous Flow Using Packed Bed Reactors
Verdier, Rasmus A. T.,Mikkelsen, Jesper H.,Lindhardt, Anders T.
, p. 1524 - 1533 (2018)
Conditions for the Morita-Baylis-Hillman reaction were developed under continuous flow using a packed bed reactor carrying 4-(dimethylamino)pyridine immobilized on silica. High reaction rates were obtained, as the packed bed reactor mimics super-stoichiom
Phosphine-catalyzed [3+2] cycloaddition of Morita—Baylis—Hillman carbonates to isothiocyanates in the synthesis of adamantane-containing trisubstituted aminothiophenes
Abel, A. S.,Averin, A. D.,Beletskaya, I. P.,Butov, G. M.,Zenkov, I. S.
, p. 880 - 884 (2021/06/07)
An addition of the Morita—Baylis—Hillman (MBH) carbonates to adamantane-containing isothiocyanates was studied. The MBH carbonates react with 1-(4-isothiocyanatophenyl)-adamantane in the presence of triphenylphosphine to give 5-aryl-substituted adamantane
Azidophosphonium salt-directed chemoselective synthesis of (E)/(Z)-cinnamyl-1H-Triazoles and regiospecific access to bromomethylcoumarins from Morita-Baylis-Hillman adducts
Karthikeyan, Soundararajan,Shobana, Radha Krishnan,Subimol, Kamarajapurathu Raju,Helen Ratna Monica,Kumar, Ayyanoth Karthik Krishna
, p. 1579 - 1587 (2020/09/16)
The direct transformation of Morita-Baylis-Hillman (MBH) adducts into molecules of interest is a crucial process wherein allylic hydroxy-protected or halogenated MBH adducts are commonly preferred. Herein, we report an azidophosphonium salt (AzPS)-catalys
