17266-44-3 Usage
General Description
Ethyl 2-(5-bromobenzo[b]thiophen-3-yl)acetate is a chemical compound that belongs to the class of esters. It is derived from the combination of ethyl alcohol and acetic acid, with the addition of a 5-bromobenzo[b]thiophene moiety. Ethyl 2-(5-bromobenzo[b]thiophen-3-yl)acetate is commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds due to its potential biological and chemical properties. It is known for its aromatic and heterocyclic structure, which provides it with unique reactivity and potential applications in various research and industrial settings. Ethyl 2-(5-bromobenzo[b]thiophen-3-yl)acetate has the potential to be used as a building block in the development of diverse organic compounds, making it an important chemical in the field of organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 17266-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17266-44:
(7*1)+(6*7)+(5*2)+(4*6)+(3*6)+(2*4)+(1*4)=113
113 % 10 = 3
So 17266-44-3 is a valid CAS Registry Number.
17266-44-3Relevant articles and documents
Substituted benzothieno [2,3-c] tetrahydropyridine derivative and preparation method and application thereof
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Paragraph 0055; 0063; 0064, (2018/07/30)
The invention belongs to the technical field of medicinal chemistry and medicines, and relates to a substituted benzothieno [2,3-c] tetrahydropyridine derivative as shown in formula (I), a preparationmethod of the substituted benzothieno [2,3-c] tetrahydr
5-Amidinobenzo[b]thiophenes as dual inhibitors of factors IXa and Xa
Qiao, Jennifer X.,Cheng, Xuhong,Modi, Dilip P.,Rossi, Karen A.,Luettgen, Joseph M.,Knabb, Robert M.,Jadhav, Prabhakar K.,Wexler, Ruth R.
, p. 29 - 35 (2007/10/03)
Syntheses and SAR studies of 5-amidinobenzo[b]thiophene analogs provided compounds with low submicromolar factor IXa potency and equal or slightly better selectivity relative to factor Xa. Syntheses and SAR studies of 5-amidinobenzo[b]thiophene analogs provided compounds with low submicromolar factor IXa activity and equal or slightly better selectivity relative to factor Xa.