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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, 3,5-diiodo-

O=Cc1cc(I)cc(c1)I Request for Quotation
Chemical Name: Benzaldehyde, 3,5-diiodo-
CAS Number: 17352-25-9
Product Number: AG001YZ5(AGN-PC-0N13PK)
Synonyms:
MDL No:
Molecular Formula: C7H4I2O
Molecular Weight: 357.9150

Identification/Properties

Computed Properties
Molecular Weight:
357.917g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
357.835g/mol
Monoisotopic Mass:
357.835g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
117
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#:
-
Hazard Statements:
H319-H317
Precautionary Statements:
P305+P351+P338-P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Diiodobenzaldehyde is a versatile compound that finds wide application in chemical synthesis as a key building block. Due to its unique structure and reactivity, this compound is utilized in the preparation of various organic compounds and complex molecules. One prominent use of 3,5-Diiodobenzaldehyde is in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. In organic chemistry, it serves as a valuable precursor for the introduction of functional groups such as aldehydes, phenyl rings, and iodine atoms into molecular structures. Additionally, 3,5-Diiodobenzaldehyde acts as an important intermediate in the synthesis of dyes, pigments, and fine chemicals. Its ability to undergo diverse reactions, such as nucleophilic substitutions and cross-coupling reactions, makes it a highly sought-after compound in the field of chemical synthesis. Overall, 3,5-Diiodobenzaldehyde plays a crucial role in enabling the efficient and practical synthesis of a wide range of valuable compounds for various industrial applications.