105189-44-4 Usage
Uses
Used in Organic Synthesis:
3,5-Dibromotyrosine trifluoroacetamide methyl ester is used as a building block or intermediate in organic synthesis for the creation of various bioactive compounds. Its unique structure allows for the development of new chemical entities with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3,5-Dibromotyrosine trifluoroacetamide methyl ester is used as a research tool to explore its potential as a therapeutic agent. Its unique chemical properties may contribute to the development of new drugs with novel mechanisms of action.
Used in Drug Discovery and Development:
3,5-Dibromotyrosine trifluoroacetamide methyl ester is utilized as a valuable tool in drug discovery and development. Its potential as a building block for the synthesis of bioactive compounds makes it a promising candidate for the creation of new therapeutic agents with diverse applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 105189-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,8 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105189-44:
(8*1)+(7*0)+(6*5)+(5*1)+(4*8)+(3*9)+(2*4)+(1*4)=114
114 % 10 = 4
So 105189-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H10Br2F3NO4/c1-22-10(20)8(18-11(21)12(15,16)17)4-5-2-6(13)9(19)7(14)3-5/h2-3,8,19H,4H2,1H3,(H,18,21)
105189-44-4Relevant academic research and scientific papers
Pyridyl and pyridazinyl substituted thyronine compounds having selective thyromimetic activity
-
, (2008/06/13)
This invention relates to chemical compounds which have selective thyromimetic activity. A compound of this invention is 3,5-dibromo-3''-[6-oxo-3(1H)-pyridazinylmethyl]-thyronine.
Formation of Quinol Ethers using (Diacetoxyiodo)benzene
Lewis, Norman,Wallbank, Philip
, p. 1103 - 1106 (2007/10/02)
The use of (diacetoxyiodo)benzene for the oxidative coupling of a hindered phenol with aliphatic alcohols or other phenols has been investigated.