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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)-

2-Thiophenecarboxaldehyde, 4-iodo-

Ic1cc(sc1)C=O Request for Quotation
Chemical Name: 2-Thiophenecarboxaldehyde, 4-iodo-
CAS Number: 18812-38-9
Product Number: AG002GQE(AGN-PC-03FB5S)
Synonyms:
MDL No:
Molecular Formula: C5H3IOS
Molecular Weight: 238.0462

Identification/Properties

Properties
BP:
298.0±25.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
238.042g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
237.895g/mol
Monoisotopic Mass:
237.895g/mol
Topological Polar Surface Area:
45.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
96.4
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Iodothiophene-2-carbaldehyde is a versatile chemical compound widely utilized in organic synthesis due to its unique reactivity and functional group compatibility. In the field of chemical synthesis, this compound serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and materials. Its ability to undergo diverse chemical transformations makes it a valuable intermediate in the synthesis of complex molecules.One of the key applications of 4-Iodothiophene-2-carbaldehyde is in the construction of heterocyclic compounds. By reacting with different nucleophiles and electrophiles, this compound can participate in a range of synthetic reactions such as Suzuki coupling, Heck reaction, and Sonogashira coupling. These reactions enable the functionalization of the thiophene ring, leading to the formation of new carbon-carbon and carbon-heteroatom bonds.Furthermore, 4-Iodothiophene-2-carbaldehyde can be used as a precursor for the synthesis of various functionalized thiophene derivatives, which have shown promising biological activities and materials properties. Its ability to introduce the iodo functionality allows for further derivatization through cross-coupling reactions, providing access to structurally diverse molecules.Overall, the strategic placement of the iodo group in 4-Iodothiophene-2-carbaldehyde offers chemists a versatile tool for designing and synthesizing novel compounds with potential applications in drug discovery, materials science, and other research areas.