31135-55-4 Usage
Description
(2S)-2-amino-3-[3,5-diiodo-4-(3-iodo-4-sulfooxy-phenoxy)phenyl]propanoic acid is a complex organic compound characterized by its unique molecular structure featuring multiple iodine atoms and a sulfooxy group. This molecule exhibits properties that make it potentially useful in various applications across different industries.
Uses
Used in Pharmaceutical Applications:
(2S)-2-amino-3-[3,5-diiodo-4-(3-iodo-4-sulfooxy-phenoxy)phenyl]propanoic acid is used as an active pharmaceutical ingredient for its potential therapeutic effects. The presence of iodine atoms and the sulfooxy group may contribute to its biological activity, making it a candidate for the development of new drugs targeting specific medical conditions.
Used in Chemical Research:
In the field of chemical research, (2S)-2-amino-3-[3,5-diiodo-4-(3-iodo-4-sulfooxy-phenoxy)phenyl]propanoic acid can be utilized as a starting material or a building block for the synthesis of more complex molecules with diverse applications. Its unique structure may offer new insights into chemical reactions and mechanisms.
Used in Analytical Chemistry:
Due to its distinct structural features, (2S)-2-amino-3-[3,5-diiodo-4-(3-iodo-4-sulfooxy-phenoxy)phenyl]propanoic acid can be employed as a reference compound or a standard in analytical chemistry. It may be used to calibrate instruments, validate analytical methods, or as a comparative benchmark in various chemical analyses.
Used in Material Science:
The unique properties of (2S)-2-amino-3-[3,5-diiodo-4-(3-iodo-4-sulfooxy-phenoxy)phenyl]propanoic acid, such as its molecular structure and functional groups, may find applications in the development of new materials with specific characteristics. It could be used as a component in the creation of advanced materials for various industries, including electronics, aerospace, or biomedical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 31135-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,3 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31135-55:
(7*3)+(6*1)+(5*1)+(4*3)+(3*5)+(2*5)+(1*5)=74
74 % 10 = 4
So 31135-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H12I3NO7S/c16-9-6-8(1-2-13(9)26-27(22,23)24)25-14-10(17)3-7(4-11(14)18)5-12(19)15(20)21/h1-4,6,12H,5,19H2,(H,20,21)(H,22,23,24)/t12-/m0/s1
31135-55-4Relevant articles and documents
Halogen bonding controls the regioselectivity of the deiodination of thyroid hormones and their sulfate analogues
Manna, Debasish,Mondal, Santanu,Mugesh, Govindasamy
supporting information, p. 2409 - 2416 (2015/01/30)
The type 1 iodothyronine deiodinase (1D-1) in liver and kidney converts the L-thyroxine (T4), a prohormone, by outer-ring (5′) deiodination to biologically active 3,3′,5-triiodothyronine (T3) or by inner-ring (5) deiodination to inactive 3,3′,5′'-triiodothronine (rT3). Sulfate conjugation is an important step in the irreversible inactivation of thyroid hormones. While sulfate conjugation of the phenolic hydroxyl group stimulates the 5-deiodination of T4 and T3, it blocks the 5′-deiodination of T4. We show that thyroxine sulfate (T4S) undergoes faster deiodination as compared to the parent thyroid hormone T4 by synthetic selenium compounds. It is also shown that ID-3 mimics, which are remarkably selective to the inner-ring deiodination of T4 and T3, changes the selectivity completely when T4S is used as a substrate. From the theoretical investigations, it is observed that the strength of halogen bonding increases upon sulfate conjugation, which leads to a change in the regioselectivity of ID-3 mimics towards the deiodination of T4S. It has been shown that these mimics perform both the 5′- and 5-ring deiodinations by an identical mechanism.
