115957-22-7 Usage
General Description
3-(2-Thienyl)-3-[(2,2,2-trifluoroacetyl)amino]propanoic acid is a chemical compound with the molecular formula C12H11F3NO3S. It is a derivative of propanoic acid and contains a thienyl group and a trifluoroacetyl group. 3-(2-THIENYL)-3-[(2,2,2-TRIFLUOROACETYL)AMINO]PROPANOIC ACID is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It has potential applications in the treatment of various diseases and disorders due to its ability to modulate biological processes. Additionally, it can also be used as a research tool in the study of chemical reactions and mechanisms. Overall, 3-(2-Thienyl)-3-[(2,2,2-trifluoroacetyl)amino]propanoic acid is a versatile compound with a wide range of potential uses in the fields of medicine and chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 115957-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,9,5 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115957-22:
(8*1)+(7*1)+(6*5)+(5*9)+(4*5)+(3*7)+(2*2)+(1*2)=137
137 % 10 = 7
So 115957-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8F3NO3S/c10-9(11,12)8(16)13-5(4-7(14)15)6-2-1-3-17-6/h1-3,5H,4H2,(H,13,16)(H,14,15)/p-1/t5-/m1/s1
115957-22-7Relevant articles and documents
Aminothiaindanone as an Accessible Scaffold for a Three-Point Chemical Diversity
Zipfel, Pauline,Lalut, Julien,Sopková-De Oliveira Santos, Jana,Rochais, Christophe,Dallemagne, Patrick
, p. 3799 - 3814 (2021/07/25)
Aminothiaindanone heterocycle appears to be a scaffold of interest in medicinal chemistry. To increase the chemical diversity in this series, the introduction of three-point chemical diversity on the cyclopenta[ b ]thiophen-4-one scaffold was explored. About thirty newly functionalized thiophene-containing bicycles were obtained using various chemical reactions, paving the way for novel possibilities in medicinal chemistry projects.
Efficient synthesis of 2-aryl-6-methyl-2,3-dihydro-1H-pyridin-4-ones
Renault, Olivier,Guillon, Jean,Dallemagne, Patrick,Rault, Sylvain
, p. 681 - 683 (2007/10/03)
Syntheses of 2-aryl-6-methyl-2,3-dihydro-1H-pyridin-4-ones were achieved starting from corresponding β-arylβ-amino acids. This reaction sequence involved, as a key step, the condensation of an acid chloride with a diketone using SmI3 as catalyst. A final intramolecular cyclization furnished the attempted product. (C) 2000 Elsevier Science Ltd.
