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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)-

Benzaldehyde, 4-hydroxy-3,5-diiodo-

O=Cc1cc(I)c(c(c1)I)O Request for Quotation
Chemical Name: Benzaldehyde, 4-hydroxy-3,5-diiodo-
CAS Number: 1948-40-9
Product Number: AG0033JF(AGN-PC-0BSKBI)
Synonyms:
MDL No:
Molecular Formula: C7H4I2O2
Molecular Weight: 373.9144

Identification/Properties

Properties
MP:
202-203°C
Storage:
Light sensitive;Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Air & Light Sensitive
Computed Properties
Molecular Weight:
373.916g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
373.83g/mol
Monoisotopic Mass:
373.83g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
139
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

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Diiodo-4-Hydroxybenzaldehyde is a key chemical reagent utilized in various chemical synthesis processes, particularly in the field of organic chemistry. This compound plays a crucial role as a building block in the creation of diverse organic molecules due to its unique structural properties.One prominent application of 3,5-Diiodo-4-Hydroxybenzaldehyde is its use as a versatile starting material for the synthesis of pharmaceutical compounds. By serving as a key intermediate, this compound enables the creation of complex molecules with specific biological activities. Its ability to undergo various chemical transformations allows for the development of novel drug candidates and therapeutic agents.Furthermore, 3,5-Diiodo-4-Hydroxybenzaldehyde has found utility in the synthesis of advanced materials such as liquid crystals and polymers. Its functional groups and reactivity make it a valuable component for designing materials with tailored properties, including optical, electrical, and mechanical characteristics. This compound's role in material science highlights its significance in advancing technology and innovation.Overall, 3,5-Diiodo-4-Hydroxybenzaldehyde serves as a fundamental building block in chemical synthesis, enabling the creation of diverse organic molecules with applications across pharmaceuticals, materials science, and other scientific fields.