19039-15-7 Usage
Description
2-(4-HYDROXY-3-IODOPHENYL)ACETIC ACID, also known as 3-Iodo-4-hydroxyphenylacetic Acid, is an organic compound that serves as an intermediate in the synthesis of various compounds. It is characterized by the presence of an iodine atom and hydroxyl group attached to a phenyl ring, with an acetic acid group connected to the 2nd carbon. This unique structure endows it with potential applications in different fields, particularly in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Industry:
2-(4-HYDROXY-3-IODOPHENYL)ACETIC ACID is used as an intermediate in the synthesis of Thyroxine (T425600) derivatives for their potential effect towards the maintenance of metabolic homeostasis. Thyroxine is a crucial hormone that plays a significant role in regulating the body's metabolism, and its derivatives may help in managing conditions related to metabolic imbalances.
Used in Chemical Synthesis:
In the chemical industry, 2-(4-HYDROXY-3-IODOPHENYL)ACETIC ACID can be utilized as a building block for the development of new compounds with various applications. Its unique structure, containing an iodine atom and hydroxyl group, allows for further chemical modifications and the creation of novel molecules with potential uses in different sectors, such as agriculture, materials science, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 19039-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,3 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19039-15:
(7*1)+(6*9)+(5*0)+(4*3)+(3*9)+(2*1)+(1*5)=107
107 % 10 = 7
So 19039-15-7 is a valid CAS Registry Number.
19039-15-7Relevant articles and documents
A Modular Access to (±)-Tubocurine and (±)-Curine - Formal Total Synthesis of Tubocurarine
Otto, Nicola,Ferenc, Dorota,Opatz, Till
, p. 1205 - 1217 (2018/06/18)
Two consecutive Cu-catalyzed Ullmann-type C-O couplings permitted the first successful entry toward the curare alkaloids (±)-tubocurine and (±)-curine. Starting from vanillin, the synthetic sequence comprises 15 linear steps and includes a total of 24 transformations. In addition, the total synthesis of tubocurine represents a formal total synthesis of the famous arrow poison alkaloid tubocurarine.
