2160-89-6 Usage
Description
1,1,1,3,3,3-Hexafluoroisopropyl acrylate is a clear colorless liquid that is used in various industries due to its unique chemical properties.
Uses
Used in Agrochemical Industry:
1,1,1,3,3,3-Hexafluoroisopropyl acrylate is used as an intermediate in the synthesis of agrochemicals for its ability to enhance the effectiveness and stability of these products.
Used in Pharmaceutical Industry:
1,1,1,3,3,3-Hexafluoroisopropyl acrylate is used as a building block in the development of pharmaceutical compounds, contributing to the creation of new drugs with improved properties.
Used in Dye Industry:
1,1,1,3,3,3-Hexafluoroisopropyl acrylate is used as a key component in the production of dyes, providing unique color characteristics and improved performance in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2160-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2160-89:
(6*2)+(5*1)+(4*6)+(3*0)+(2*8)+(1*9)=66
66 % 10 = 6
So 2160-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F6O2/c1-2-3(13)14-4(5(7,8)9)6(10,11)12/h2,4H,1H2
2160-89-6Relevant articles and documents
DIELS-ALDER REACTION WITH FURANICS TO OBTAIN AROMATICS
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Page/Page column 11-12, (2020/03/23)
The present invention is directed to the preparation of phthalic anhydride compounds and the intermediate phthalide compounds. In particular, the invention is directed to an improved bio-based route from furanic compounds to phthalic anhydride compounds by reacting furfuryl alcohol (i.e. 2-hydroxymethylfuran) or an analogue thereof having a nucleophilic atom on the 2-methyl, with a dienophile comprising an α,β-unsaturated carbonyl comprising an α'-leaving group. The inventions further involved preparation of phthalic anhydride compounds, phthalic acid compounds and reduction products of the intermediate phthalide compounds.