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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Thyroxine-4-hydroxy-3,5-diiodophenyl Ether

OC(=O)[C@H](Cc1cc(I)c(c(c1)I)Oc1cc(I)c(c(c1)I)Oc1cc(I)c(c(c1)I)O)N Request for Quotation
Chemical Name: Thyroxine-4-hydroxy-3,5-diiodophenyl Ether
CAS Number: 911661-90-0
Product Number: AG0036SP(AGN-PC-0WAHS4)
Synonyms:
MDL No:
Molecular Formula: C21H13I6NO5
Molecular Weight: 1120.7584

Identification/Properties

Properties
Storage:
2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, O-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]-3,5-diiodo-L-tyrosine plays a crucial role as a versatile building block. With its unique structure consisting of multiple iodine and hydroxy groups, this compound serves as a valuable precursor in the creation of complex organic molecules. Its dual functionality allows for the introduction of iodine atoms at specific positions within the target molecule, enabling precise modifications during synthetic processes. Additionally, the phenolic hydroxy group provides opportunities for further derivatization, expanding the compound's utility in diverse chemical reactions. By incorporating O-[4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]-3,5-diiodo-L-tyrosine into various synthetic pathways, chemists can access new avenues for the synthesis of advanced materials, pharmaceuticals, and bioactive compounds.