58110-39-7 Usage
Uses
Used in Pharmaceutical Industry:
(2E)-3-[5-(2-CHLOROPHENYL)-2-FURYL]PROP-2-ENOIC ACID is used as a synthetic intermediate for the development of new drugs. Its unique structure and reactivity make it a promising candidate for the creation of pharmaceutical compounds with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, (2E)-3-[5-(2-CHLOROPHENYL)-2-FURYL]PROP-2-ENOIC ACID is utilized as a building block in the production of agrochemicals. Its potential applications in this field include the development of new pesticides, herbicides, and other agricultural chemicals that can improve crop yields and protect plants from pests.
Used in Specialty Chemicals Production:
(2E)-3-[5-(2-CHLOROPHENYL)-2-FURYL]PROP-2-ENOIC ACID is also used in the manufacturing of various specialty chemicals. Its versatility and unique combination of functional groups make it an essential component in the synthesis of compounds with specific properties, which can be applied in different industries such as coatings, plastics, and materials science.
Used in Organic Synthesis:
As a valuable and versatile component in organic synthesis, (2E)-3-[5-(2-CHLOROPHENYL)-2-FURYL]PROP-2-ENOIC ACID is employed for further derivatization to create new compounds with specific properties and applications. Its reactivity and functional groups provide opportunities for the development of innovative chemical products and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 58110-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58110-39:
(7*5)+(6*8)+(5*1)+(4*1)+(3*0)+(2*3)+(1*9)=107
107 % 10 = 7
So 58110-39-7 is a valid CAS Registry Number.
58110-39-7Relevant academic research and scientific papers
2-amino-3-(5-phenylfuran-2-yl)propionic acids and 5-phenylfuran-2-ylacrylic acids are novel substrates of phenylalanine ammonia-lyase
Paizs, Csaba,Tosa, Monica Ioana,Bencze, Laszlo Csaba,Brem, Juergen,Irimie, Florin Dan,Retey, Janos
, p. 1217 - 1228 (2011/05/05)
Both racemic 2-amino-3-(5-phenylfuran-2-yl)propionic acids and 5-phenylfuran-2-ylacrylic acids were synthesized and spectroscopically characterized (UV, EI-MS, 1H-NMR and 13C-NMR). The phenyl group of the 5-phenylfuranyl residue carried no (rac-la) para-Br (rac-lb) or Cl para or ortho (rac-lc, d) substituents. The novel furanylalanines were used as substrates of recombinant phenylalanine ammonia-lyase (PAL). When 50% of the racemic 5-phenylfuranylalanines were converted into the corresponding acrylates, the D-enantiomers of the substrates could be isolated. The L-enantiomers could be prepared from the substituted acrylates when the PAL reaction was reversed in the presence of 6 M ammonia at pH 10. The Japan Institute of Heterocyclic Chemistry.
