58110-39-7 Usage
General Description
The chemical compound, (2E)-3-[5-(2-chlorophenyl)-2-furyl]prop-2-enoic acid, is a synthetic organic compound consisting of a furan ring, a phenyl ring with a chlorine substituent, and a propenoic acid group. It is commonly used as a synthetic intermediate or building block in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. The compound has potential applications in the development of new drugs, as well as in the manufacturing of various chemical products. Its structure and reactivity make it a valuable and versatile component in organic synthesis. Additionally, its unique combination of functional groups provides opportunities for further derivatization to create new compounds with specific properties and applications.
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 articles and documents
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.