329915-01-7 Usage
Uses
Used in Organic Synthesis:
(E)-1,1,1-trifluoro-4-(phenylsulfonyl)but-3-ene-2,2-diol is used as a building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its diverse functional groups allow for a wide range of reactions and modifications, making it a valuable component in the creation of complex molecules.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (E)-1,1,1-trifluoro-4-(phenylsulfonyl)but-3-ene-2,2-diol is used as a target compound for the development of new bioactive molecules. The presence of the trifluoromethyl and phenylsulfonyl groups, which are commonly found in bioactive molecules, makes (E)-1,1,1-trifluoro-4-(phenylsulfonyl)but-3-ene-2,2-diol particularly attractive for research aimed at discovering novel therapeutic agents.
Used in Pharmaceutical Industry:
(E)-1,1,1-trifluoro-4-(phenylsulfonyl)but-3-ene-2,2-diol is used as a key intermediate in the development of new drugs. Its unique structure and reactivity enable the creation of pharmaceuticals with specific therapeutic properties, contributing to the advancement of treatments for various diseases and conditions.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (E)-1,1,1-trifluoro-4-(phenylsulfonyl)but-3-ene-2,2-diol is utilized as a starting material for the synthesis of new agrochemicals. Its functional groups can be tailored to create compounds with targeted effects on pests or crops, potentially leading to more effective and environmentally friendly products.
Check Digit Verification of cas no
The CAS Registry Mumber 329915-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,9,1 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 329915-01:
(8*3)+(7*2)+(6*9)+(5*9)+(4*1)+(3*5)+(2*0)+(1*1)=157
157 % 10 = 7
So 329915-01-7 is a valid CAS Registry Number.
329915-01-7Relevant academic research and scientific papers
Synthesis of β-trifluoroacetyl-substituted vinyl sulfones and vinyl sulfides
Krasovsky,Nenajdenko,Balenkova
, p. 2080 - 2085 (2007/10/03)
Oxidation of β-(trifluoroacetyl)vinyl sulfides afforded a series of the corresponding sulfones. The reactions of sulfones with various alkyl- and arylthiols were studied. These reactions provide the basis for a new procedure for the synthesis of β-(trifluoroacetyl)vinyl sulfides.
A novel efficient synthesis of heteroaryl substituted α,β-unsaturated trifluoromethyl ketones
Nenajdenko, Valentine G.,Krasovsky, Arkady L.,Lebedev, Mikhail V.,Balenkova, Elizabeth S.
, p. 1349 - 1350 (2007/10/03)
A synthesis of a novel electrophilic reagent 1,1,1-trifluoro-4-(phenylsulfonyl)-but-3-ene-2,2-diol 2 is described. The reaction of 2 with various electron-rich heteroaromatics such as furans, pyrroles, indoles is investigated. The addition-elimination reaction proceeds under mild conditions stereospecifically and permits a novel one-step procedure for the preparation of trifluoroacetylvinyl substituted heterocycles in high yield. In all cases only E-isomers of unsaturated CF3 ketones were obtained.
