1. Home
  2. Benzoic acid, 4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodo-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Benzoic acid, 4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodo-

OC(=O)c1cc(I)c(c(c1)I)Oc1cc(I)c(c(c1)I)O Request for Quotation
Chemical Name: Benzoic acid, 4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodo-
CAS Number: 2055-97-2
Product Number: AG002A4L(AGN-PC-0LTM0A)
Synonyms:
MDL No:
Molecular Formula: C13H6I4O4
Molecular Weight: 733.8022

Identification/Properties

Properties
MP:
>230°C (dec.)
Storage:
2-8℃;Light sensitive;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
733.805g/mol
XLogP3:
5.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
733.644g/mol
Monoisotopic Mass:
733.644g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
359
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Tetraiodothyroformic acid is a valuable compound in chemical synthesis due to its unique properties and versatile applications. As a strong acid, it can be utilized as a powerful catalyst in various organic reactions, particularly in the formation of carbon-carbon bonds. Its high reactivity and stability make it a preferred choice for promoting complex transformations in the laboratory setting. Additionally, Tetraiodothyroformic acid serves as an effective tool in the preparation of pharmaceutical intermediates and specialty chemicals, contributing to advancements in drug discovery and materials science. Its precise structure and controlled reactivity enable precise control over reaction pathways, leading to the efficient synthesis of target molecules with high purity and yield. In summary, Tetraiodothyroformic acid plays a crucial role in enabling chemists to explore new synthetic routes and develop innovative compounds with diverse applications.